CTD Diseases (CD): Intellectual Disability

Root: CD Hierarchy (CTD diseases from Comparative Toxicogenomics Database)

Shortest distance to current term (+ for parents, - for children)	CD term [CD ID] <#Children>	#Domains (Superfamily|Family)	#Supra-domain (Single|Duplex|Triple)
+ + + + 4:	Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>	(81|94)	(88|48|16)
+ + + 3:	Diseases [MESH:C] <25>
+ + + 3:	Nervous System Diseases [MESH:D009422] <27>	(86|87)	(91|33|8)
+ + + 3:	Signs and Symptoms [MESH:D012816] <38>	(30|33)	(33|13|1)
+ + 2:	Mental Disorders [MESH:D001523] <27>	(22|26)	(25|8|3)
+ + 2:	Neurologic Manifestations [MESH:D009461] <26>	(22|24)	(25|9|1)
+ 1:	Neurobehavioral Manifestations [MESH:D019954] <10>	(5|5)	(5|1|0)
+ 1:	Neurodevelopmental Disorders [MESH:D065886] <17>	(9|11)	(12|5|2)
0:	Intellectual Disability [MESH:D008607] <521>	(2|2)	(2|1|0)
- 1:	Mental Retardation, X-Linked [MESH:D038901] <128>	(0|0)	(0|0|0)
- 1:	Cri-du-Chat Syndrome [MESH:D003410] <6>	(0|0)	(0|0|0)
- 1:	Down Syndrome [MESH:D004314] <6>	(1|0)	(1|0|0)
- 1:	Fryns-Aftimos Syndrome [MESH:C565258] <2>	(0|0)	(0|0|0)
- 1:	Prader-Willi Syndrome [MESH:D011218] <2>	(0|0)	(0|0|0)
- 1:	Rubinstein-Taybi Syndrome [MESH:D012415] <2>	(0|0)	(0|0|0)
- 1:	Spastic Ataxia [MESH:C564815] <2>	(0|0)	(0|0|0)
- 1:	WAGR Syndrome [MESH:D017624] <2>	(0|0)	(0|0|0)
- 1:	15q24 Microdeletion [MESH:C579849] <1>	(0|0)	(0|0|0)
- 1:	De Lange Syndrome [MESH:D003635] <1>	(0|0)	(0|0|0)
- 1:	Hyperphosphatasia with Mental Retardation [MESH:C565495] <1>	(0|0)	(0|0|0)
- 1:	NF1 Microdeletion Syndrome [MESH:C563524] <1>	(0|0)	(0|0|0)
- 1:	Pitt-Hopkins syndrome [MESH:C537403] <1>	(0|0)	(0|0|0)
- 1:	Sketetal dysplasia coarse facies mental retardation [MESH:C536671] <1>	(0|0)	(0|0|0)
- 1:	Williams Syndrome [MESH:D018980] <1>	(0|0)	(0|0|0)
- 1:	16p11.2 Deletion Syndrome [MESH:C579850]	(0|0)	(0|0|0)
- 1:	AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency [MESH:C563876]	(0|0)	(0|0|0)
- 1:	AL-RAQAD SYNDROME [OMIM:616459]	(0|0)	(0|0|0)
- 1:	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME [OMIM:615510]	(0|0)	(0|0|0)
- 1:	ALAZAMI SYNDROME [OMIM:615071]	(0|0)	(0|0|0)
- 1:	ALAZAMI-YUAN SYNDROME [OMIM:617126]	(0|0)	(0|0|0)
- 1:	ALOPECIA-MENTAL RETARDATION SYNDROME 3 [OMIM:613930]	(0|0)	(0|0|0)
- 1:	AMR Syndrome [MESH:C565965]	(0|0)	(0|0|0)
- 1:	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES [OMIM:615553]	(0|0)	(0|0|0)
- 1:	AU-KLINE SYNDROME [OMIM:616580]	(0|0)	(0|0|0)
- 1:	Absent Eyebrows and Eyelashes with Mental Retardation [MESH:C563111]	(0|0)	(0|0|0)
- 1:	Acrodysostosis [MESH:C538179]	(0|0)	(0|0|0)
- 1:	Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital [MESH:C563429]	(0|0)	(0|0|0)
- 1:	Akesson syndrome [MESH:C535610]	(0|0)	(0|0|0)
- 1:	Al Gazali Aziz Salem syndrome [MESH:C535613]	(0|0)	(0|0|0)
- 1:	Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus [MESH:C565968]	(0|0)	(0|0|0)
- 1:	Alopecia contractures dwarfism mental retardation [MESH:C537051]	(0|0)	(0|0|0)
- 1:	Alopecia epilepsy oligophrenia syndrome of Moynahan [MESH:C537052]	(0|0)	(0|0|0)
- 1:	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome [MESH:C567425]	(0|0)	(0|0|0)
- 1:	Alopecia, epilepsy, pyorrhea, mental subnormality [MESH:C537057]	(0|0)	(0|0|0)
- 1:	Alopecia-Mental Retardation Syndrome 2 [MESH:C563668]	(0|0)	(0|0|0)
- 1:	Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism [MESH:C563370]	(0|0)	(0|0|0)
- 1:	Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type [MESH:C563050]	(0|0)	(0|0|0)
- 1:	Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis [MESH:C564570]	(0|0)	(0|0|0)
- 1:	Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis [MESH:C565960]	(0|0)	(0|0|0)
- 1:	Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation [MESH:C565958]	(0|0)	(0|0|0)
- 1:	Amyotrophic Dystonic Paraplegia [MESH:C566292]	(0|0)	(0|0|0)
- 1:	Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies-Mental Retardation Syndrome [MESH:C565796]	(0|0)	(0|0|0)
- 1:	Aniridia cerebellar ataxia mental deficiency [MESH:C536370]	(0|0)	(0|0|0)
- 1:	Ansell Bywaters Elderking syndrome [MESH:C537773]	(0|0)	(0|0|0)
- 1:	Aortic arch anomaly with peculiar facies and mental retardation [MESH:C537785]	(0|0)	(0|0|0)
- 1:	Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV [MESH:C563942]	(0|0)	(0|0|0)
- 1:	Arachnodactyly ataxia cataract aminoaciduria mental retardation [MESH:C537424]	(0|0)	(0|0|0)
- 1:	Arginine-Glycine Amidinotransferase Deficiency [MESH:C567192]	(0|0)	(0|0|0)
- 1:	Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies [MESH:C565940]	(0|0)	(0|0|0)
- 1:	Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies [MESH:C535385]	(0|0)	(0|0|0)
- 1:	Aughton syndrome [MESH:C538269]	(0|0)	(0|0|0)
- 1:	Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation [MESH:C565923]	(0|0)	(0|0|0)
- 1:	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME [OMIM:616449]	(0|0)	(0|0|0)
- 1:	BEAULIEU-BOYCOTT-INNES SYNDROME [OMIM:613680]	(0|0)	(0|0|0)
- 1:	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME [OMIM:615722]	(0|0)	(0|0|0)
- 1:	BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY [OMIM:614923]	(0|0)	(0|0|0)
- 1:	Baraitser Rodeck Garner syndrome [MESH:C537906]	(0|0)	(0|0|0)
- 1:	Battaglia Neri syndrome [MESH:C537662]	(0|0)	(0|0|0)
- 1:	Behr syndrome [MESH:C537669]	(0|0)	(0|0|0)
- 1:	Bellini Chiumello Rimoldi syndrome [MESH:C535652]	(0|0)	(0|0|0)
- 1:	Biemond syndrome II [MESH:C565902]	(0|0)	(0|0|0)
- 1:	Birk-Barel Mental Retardation Dysmorphism Syndrome [MESH:C567357]	(0|0)	(0|0|0)
- 1:	Blepharophimosis syndrome Ohdo type [MESH:C536232]	(0|0)	(0|0|0)
- 1:	Blepharophimosis with Facial and Genital Anomalies and Mental Retardation [MESH:C565797]	(0|0)	(0|0|0)
- 1:	Bohring syndrome [MESH:C537419]	(0|0)	(0|0|0)
- 1:	Boudhina Yedes Khiari syndrome [MESH:C537939]	(0|0)	(0|0|0)
- 1:	Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ea [MESH:C564519]	(0|0)	(0|0|0)
- 1:	Brunner Syndrome [MESH:C563156]	(0|0)	(0|0|0)
- 1:	Bullous Dystrophy, Hereditary Macular Type [MESH:C563065]	(0|0)	(0|0|0)
- 1:	CAHMR syndrome [MESH:C537959]	(0|0)	(0|0|0)
- 1:	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION [OMIM:614756]	(0|0)	(0|0|0)
- 1:	CEREBELLOFACIODENTAL SYNDROME [OMIM:616202]	(0|0)	(0|0|0)
- 1:	CHROMOSOME 13q14 DELETION SYNDROME [OMIM:613884]	(0|0)	(0|0|0)
- 1:	CHROMOSOME 17p13.1 DELETION SYNDROME [OMIM:613776]	(0|0)	(0|0|0)
- 1:	CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB [OMIM:613729]	(0|0)	(0|0|0)
- 1:	CHROMOSOME 8q21.11 DELETION SYNDROME [OMIM:614230]	(0|0)	(0|0|0)
- 1:	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION [OMIM:120433]	(0|0)	(0|0|0)
- 1:	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER [OMIM:617360]	(0|0)	(0|0|0)
- 1:	Camera Marugo Cohen syndrome [MESH:C537964]	(0|0)	(0|0|0)
- 1:	Cantalamessa Baldini Ambrosi syndrome [MESH:C537981]	(0|0)	(0|0|0)
- 1:	Cantu Sanchez-Corona Fragoso syndrome [MESH:C535571]	(0|0)	(0|0|0)
- 1:	Cartwright Nelson Fryns syndrome [MESH:C535917]	(0|0)	(0|0|0)
- 1:	Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy [MESH:C564353]	(0|0)	(0|0|0)
- 1:	Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stat [MESH:C563390]	(0|0)	(0|0|0)
- 1:	Cataracts, ataxia, short stature, and mental retardation [MESH:C535345]	(0|0)	(0|0|0)
- 1:	Cephalin Lipidosis [MESH:C565872]	(0|0)	(0|0|0)
- 1:	Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 [MESH:C567656]	(0|0)	(0|0|0)
- 1:	Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 [MESH:C567690]	(0|0)	(0|0|0)
- 1:	Cerebral Cavernous Malformations 2 [MESH:C566394]	(0|0)	(0|0|0)
- 1:	Cerebral Cavernous Malformations 3 [MESH:C566393]	(0|0)	(0|0|0)
- 1:	Cerebrocostomandibular Syndrome [MESH:C562538]	(0|0)	(0|0|0)
- 1:	Cerebrofaciothoracic Dysplasia [MESH:C565862]	(0|0)	(0|0|0)
- 1:	Cerebrooculofacioskeletal Syndrome 2 [MESH:C565185]	(0|0)	(0|0|0)
- 1:	Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184]	(0|0)	(0|0|0)
- 1:	Cerebrooculonasal Syndrome [MESH:C565313]	(0|0)	(0|0|0)
- 1:	Choroid plexus calcification with mental retardation [MESH:C535357]	(0|0)	(0|0|0)
- 1:	Chromosome 15q13.3 Microdeletion Syndrome [MESH:C567439]	(0|0)	(0|0|0)
- 1:	Chromosome 15q26-Qter Deletion Syndrome [MESH:C567232]	(0|0)	(0|0|0)
- 1:	Chromosome 17q21.31 Deletion Syndrome [MESH:C566476]	(0|0)	(0|0|0)
- 1:	Chromosome 18 Pericentric Inversion [MESH:C563734]	(0|0)	(0|0|0)
- 1:	Chromosome 1q21.1 Duplication Syndrome [MESH:C567290]	(0|0)	(0|0|0)
- 1:	Chromosome 1q43-Q44 Deletion Syndrome [MESH:C567346]	(0|0)	(0|0|0)
- 1:	Chromosome 2q31.2 Deletion Syndrome [MESH:C567344]	(0|0)	(0|0|0)
- 1:	Chromosome 2q32-Q33 Deletion Syndrome [MESH:C567350]	(0|0)	(0|0|0)
- 1:	Chromosome 3q29 Deletion Syndrome [MESH:C567184]	(0|0)	(0|0|0)
- 1:	Chromosome Xq28 Duplication Syndrome [MESH:C567580]	(0|0)	(0|0|0)
- 1:	Chudley-Rozdilsky syndrome [MESH:C535458]	(0|0)	(0|0|0)
- 1:	Cleft Palate, Isolated, And Mental Retardation [MESH:C566991]	(0|0)	(0|0|0)
- 1:	Coffin syndrome 1 [MESH:C536435]	(0|0)	(0|0|0)
- 1:	Coffin-Siris syndrome [MESH:C536436]	(0|0)	(0|0|0)
- 1:	Cohen syndrome [MESH:C536438]	(0|0)	(0|0|0)
- 1:	Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation [MESH:C565173]	(0|0)	(0|0|0)
- 1:	Coloboma, cleft lip-palate and mental retardation syndrome [MESH:C535971]	(0|0)	(0|0|0)
- 1:	Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome [MESH:C566623]	(0|0)	(0|0|0)
- 1:	Convulsive Disorder, Familial, with Prenatal or Early Onset [MESH:C565678]	(0|0)	(0|0|0)
- 1:	Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia [MESH:C564509]	(0|0)	(0|0|0)
- 1:	Cortical Blindness, Retardation, and Postaxial Polydactyly [MESH:C565674]	(0|0)	(0|0|0)
- 1:	Craniofaciofrontodigital Syndrome [MESH:C567298]	(0|0)	(0|0|0)
- 1:	Craniosynostosis Mental Retardation Clefting Syndrome [MESH:C565663]	(0|0)	(0|0|0)
- 1:	Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig [MESH:C565664]	(0|0)	(0|0|0)
- 1:	Cree Mental Retardation Syndrome [MESH:C564654]	(0|0)	(0|0|0)
- 1:	Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepa [MESH:C563840]	(0|0)	(0|0|0)
- 1:	Cubitus Valgus with Mental Retardation and Unusual Facies [MESH:C564510]	(0|0)	(0|0|0)
- 1:	Curatolo Cilio Pessagno syndrome [MESH:C536701]	(0|0)	(0|0|0)
- 1:	Cutis Verticis Gyrata and Mental Deficiency [MESH:C565661]	(0|0)	(0|0|0)
- 1:	Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality [MESH:C565658]	(0|0)	(0|0|0)
- 1:	Davis Lafer syndrome [MESH:C535989]	(0|0)	(0|0|0)
- 1:	De Barsy syndrome [MESH:C535990]	(0|0)	(0|0|0)
- 1:	De Sanctis-Cacchione syndrome [MESH:C535992]	(0|0)	(0|0|0)
- 1:	Deafness, Cochlear, with Myopia and Intellectual Impairment [MESH:C565645]	(0|0)	(0|0|0)
- 1:	Deafness, congenital onychodystrophy, recessive form [MESH:C538204]	(0|0)	(0|0|0)
- 1:	Devriendt syndrome [MESH:C535947]	(0|0)	(0|0|0)
- 1:	Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification [MESH:C565632]	(0|0)	(0|0|0)
- 1:	Dicarboxylicaminoaciduria [MESH:C536171]	(0|0)	(0|0|0)
- 1:	Digitorenocerebral Syndrome [MESH:C563052]	(0|0)	(0|0|0)
- 1:	Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation [MESH:C566408]	(0|0)	(0|0|0)
- 1:	Dubowitz syndrome [MESH:C535718]	(0|0)	(0|0|0)
- 1:	Duker Weiss Siber syndrome [MESH:C535719]	(0|0)	(0|0|0)
- 1:	Duplication 15q11-q13 Syndrome [MESH:C557830]	(0|0)	(0|0|0)
- 1:	Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone [MESH:C565615]	(0|0)	(0|0|0)
- 1:	Dyggve-Melchior-Clausen syndrome [MESH:C535726]	(0|0)	(0|0|0)
- 1:	Dysequilibrium syndrome [MESH:C535731]	(0|0)	(0|0|0)
- 1:	Dysmyelination With Jaundice [MESH:C565610]	(0|0)	(0|0|0)
- 1:	EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION [OMIM:245570]	(0|0)	(0|0|0)
- 1:	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME [OMIM:616577]	(0|0)	(0|0|0)
- 1:	Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum [MESH:C565605]	(0|0)	(0|0|0)
- 1:	Ectodermal dysplasia mental retardation syndactyly [MESH:C538018]	(0|0)	(0|0|0)
- 1:	Elliott Ludman Teebi syndrome [MESH:C536204]	(0|0)	(0|0|0)
- 1:	Emanuel syndrome [MESH:C535733]	(0|0)	(0|0|0)
- 1:	Emphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation [MESH:C566519]	(0|0)	(0|0|0)
- 1:	Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal [MESH:C565594]	(0|0)	(0|0|0)
- 1:	Epidermolysis bullosa, late-onset localized junctional, with mental retardation [MESH:C535492]	(0|0)	(0|0|0)
- 1:	Epilepsy telangiectasia [MESH:C535497]	(0|0)	(0|0|0)
- 1:	Epilepsy, Female-Restricted, with Mental Retardation [MESH:C564715]	(0|0)	(0|0|0)
- 1:	Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation [MESH:C565587]	(0|0)	(0|0|0)
- 1:	Facial Abnormalities, Kyphoscoliosis, and Mental Retardation [MESH:C565580]	(0|0)	(0|0|0)
- 1:	Faciocardiomelic Syndrome [MESH:C567176]	(0|0)	(0|0|0)
- 1:	Fallot complex with severe mental and growth retardation [MESH:C536608]	(0|0)	(0|0|0)
- 1:	Feingold Trainer syndrome [MESH:C536179]	(0|0)	(0|0|0)
- 1:	Fg Syndrome 5 [MESH:C564480]	(0|0)	(0|0|0)
- 1:	Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation [MESH:C565331]	(0|0)	(0|0|0)
- 1:	Filippi syndrome [MESH:C538152]	(0|0)	(0|0|0)
- 1:	Fine-Lubinsky syndrome [MESH:C537933]	(0|0)	(0|0|0)
- 1:	Fitzsimmons Walson Mellor syndrome [MESH:C537937]	(0|0)	(0|0|0)
- 1:	Fitzsimmons-McLachlan-Gilbert syndrome [MESH:C537058]	(0|0)	(0|0|0)
- 1:	Fountain syndrome [MESH:C537270]	(0|0)	(0|0|0)
- 1:	GROWTH RETARDATION, IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND HEPATOPATHY [OMIM:617093]	(0|0)	(0|0|0)
- 1:	Garret Tripp syndrome [MESH:C535646]	(0|0)	(0|0|0)
- 1:	Genitopatellar Syndrome [MESH:C565255]	(0|0)	(0|0|0)
- 1:	Goniodysgenesis-Mental Retardation-Short Stature Syndrome [MESH:C564214]	(0|0)	(0|0|0)
- 1:	Growth Deficiency and Mental Retardation with Facial Dysmorphism [MESH:C565358]	(0|0)	(0|0|0)
- 1:	Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, [MESH:C564264]	(0|0)	(0|0|0)
- 1:	Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia [MESH:C565755]	(0|0)	(0|0|0)
- 1:	Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [MESH:C537405]	(0|0)	(0|0|0)
- 1:	Growth mental deficiency syndrome of Myhre [MESH:C537620]	(0|0)	(0|0|0)
- 1:	Gurrieri Sammito Bellussi syndrome [MESH:C537625]	(0|0)	(0|0|0)
- 1:	HAREL-YOON SYNDROME [OMIM:617183]	(0|0)	(0|0|0)
- 1:	HELSMOORTEL-VAN DER AA SYNDROME [OMIM:615873]	(0|0)	(0|0|0)
- 1:	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1 [OMIM:616418]	(0|0)	(0|0|0)
- 1:	Hair defect with photosensitivity and mental retardation [MESH:C537628]	(0|0)	(0|0|0)
- 1:	Hall Riggs mental retardation syndrome [MESH:C535623]	(0|0)	(0|0|0)
- 1:	Harrod Doman Keele syndrome [MESH:C535635]	(0|0)	(0|0|0)
- 1:	Haspeslagh Fryns Muelenaere syndrome [MESH:C535844]	(0|0)	(0|0|0)
- 1:	Hittner Hirsch Kreh syndrome [MESH:C538323]	(0|0)	(0|0|0)
- 1:	Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate [MESH:C564484]	(0|0)	(0|0|0)
- 1:	Hooft disease [MESH:C535329]	(0|0)	(0|0|0)
- 1:	Hordnes Engebretsen Knudtson syndrome [MESH:C536067]	(0|0)	(0|0|0)
- 1:	Hoyeraal Hreidarsson syndrome [MESH:C536068]	(0|0)	(0|0|0)
- 1:	Hunter-McAlpine syndrome [MESH:C536072]	(0|0)	(0|0|0)
- 1:	Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardat [MESH:C565736]	(0|0)	(0|0|0)
- 1:	Hydroxylysinuria [MESH:C565502]	(0|0)	(0|0|0)
- 1:	Hyperleucine-Isoleucinemia [MESH:C562674]	(0|0)	(0|0|0)
- 1:	Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria [MESH:C565499]	(0|0)	(0|0|0)
- 1:	Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility [MESH:C566988]	(0|0)	(0|0|0)
- 1:	Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltrans [MESH:C565489]	(0|0)	(0|0|0)
- 1:	Hypogonadism with Low-Grade Mental Deficiency and Microcephaly [MESH:C565482]	(0|0)	(0|0|0)
- 1:	Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies [MESH:C564406]	(0|0)	(0|0|0)
- 1:	Hypoparathyroidism-retardation-dysmorphism syndrome [MESH:C537157]	(0|0)	(0|0|0)
- 1:	Hypospadias-Mental Retardation Syndrome [MESH:C563067]	(0|0)	(0|0|0)
- 1:	Hypotonia-Cystinuria Syndrome [MESH:C564710]	(0|0)	(0|0|0)
- 1:	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA [OMIM:617173]	(0|0)	(0|0|0)
- 1:	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS [OMIM:617333]	(0|0)	(0|0|0)
- 1:	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES [OMIM:617452]	(0|0)	(0|0|0)
- 1:	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN [OMIM:617101]	(0|0)	(0|0|0)
- 1:	Ichthyosis and male hypogonadism [MESH:C537365]	(0|0)	(0|0|0)
- 1:	Ichthyosis, mental retardation, dwarfism, and renal impairment [MESH:C536274]	(0|0)	(0|0|0)
- 1:	Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin [MESH:C563402]	(0|0)	(0|0|0)
- 1:	Indolylacroyl Glycinuria with Mental Retardation [MESH:C565466]	(0|0)	(0|0|0)
- 1:	Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation [MESH:C565462]	(0|0)	(0|0|0)
- 1:	JANSEN-DE VRIES SYNDROME [OMIM:617450]	(0|0)	(0|0|0)
- 1:	Jagell Holmgren Hofer syndrome [MESH:C537364]	(0|0)	(0|0|0)
- 1:	Johanson Blizzard syndrome [MESH:C535880]	(0|0)	(0|0|0)
- 1:	Joubert Syndrome 7 [MESH:C566916]	(0|0)	(0|0|0)
- 1:	Joubert Syndrome 9 [MESH:C567364]	(0|0)	(0|0|0)
- 1:	KBG syndrome [MESH:C537015]	(0|0)	(0|0|0)
- 1:	KEPPEN-LUBINSKY SYNDROME [OMIM:614098]	(0|0)	(0|0|0)
- 1:	Kahrizi Syndrome [MESH:C567196]	(0|0)	(0|0|0)
- 1:	Kaler Garrity Stern syndrome [MESH:C537706]	(0|0)	(0|0|0)
- 1:	Kapur Toriello syndrome [MESH:C537008]	(0|0)	(0|0|0)
- 1:	Karandikar Maria Kamble syndrome [MESH:C537009]	(0|0)	(0|0|0)
- 1:	Katsantoni Papadakou Lagoyanni syndrome [MESH:C537012]	(0|0)	(0|0|0)
- 1:	Kaufman oculocerebrofacial syndrome [MESH:C537013]	(0|0)	(0|0|0)
- 1:	Kleefstra Syndrome [MESH:C563043]	(0|0)	(0|0|0)
- 1:	Koone Rizzo Elias syndrome [MESH:C537023]	(0|0)	(0|0|0)
- 1:	Kosztolanyi syndrome [MESH:C537024]	(0|0)	(0|0|0)
- 1:	Kozlowski Ouvrier syndrome [MESH:C537508]	(0|0)	(0|0|0)
- 1:	Kozlowski Rafinski Klicharska syndrome [MESH:C537509]	(0|0)	(0|0|0)
- 1:	Kozlowski-Krajewska syndrome [MESH:C537615]	(0|0)	(0|0|0)
- 1:	Kuzniecky syndrome [MESH:C538091]	(0|0)	(0|0|0)
- 1:	LAMB-SHAFFER SYNDROME [OMIM:616803]	(0|0)	(0|0|0)
- 1:	LUSCAN-LUMISH SYNDROME [OMIM:616831]	(0|0)	(0|0|0)
- 1:	Lambert syndrome [MESH:C538396]	(0|0)	(0|0|0)
- 1:	Lenz Majewski hyperostotic dwarfism [MESH:C537115]	(0|0)	(0|0|0)
- 1:	Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis [MESH:C565440]	(0|0)	(0|0|0)
- 1:	Light Fixation Seizure Syndrome [MESH:C566367]	(0|0)	(0|0|0)
- 1:	Limb Defects, Distal Transverse, with Mental Retardation and Spasticity [MESH:C565438]	(0|0)	(0|0|0)
- 1:	Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones [MESH:C564283]	(0|0)	(0|0|0)
- 1:	Lissencephaly 3 [MESH:C566908]	(0|0)	(0|0|0)
- 1:	Lowry Maclean syndrome [MESH:C537037]	(0|0)	(0|0|0)
- 1:	Lowry Wood syndrome [MESH:C537038]	(0|0)	(0|0|0)
- 1:	Lubani Al Saleh Teebi syndrome [MESH:C537039]	(0|0)	(0|0|0)
- 1:	Lynch Lee Murday syndrome [MESH:C537713]	(0|0)	(0|0|0)
- 1:	MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome [MESH:C536029]	(0|0)	(0|0|0)
- 1:	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RET [OMIM:613926]	(0|0)	(0|0|0)
- 1:	MEND SYNDROME [OMIM:300960]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS [OMIM:616789]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES [OMIM:613670]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS [OMIM:613671]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 10 [OMIM:614256]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 11 [OMIM:614257]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 [OMIM:614563]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18 [OMIM:615074]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2 [OMIM:614113]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 [OMIM:613443]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21 [OMIM:615502]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22 [OMIM:612337]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 [OMIM:615761]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 [OMIM:615828]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 [OMIM:615834]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 [OMIM:616078]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30 [OMIM:616083]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 [OMIM:616158]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 [OMIM:616268]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 33 [OMIM:616311]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 34 [OMIM:616351]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35 [OMIM:616355]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36 [OMIM:616362]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38 [OMIM:616393]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39 [OMIM:616521]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40 [OMIM:616579]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41 [OMIM:616944]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42 [OMIM:616973]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43 [OMIM:616977]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44 [OMIM:617061]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES [OMIM:613970]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 [OMIM:614104]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 [OMIM:614255]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14 [OMIM:614020]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 [OMIM:614202]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16 [OMIM:614208]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18 [OMIM:614249]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27 [OMIM:614340]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY [OMIM:614499]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36 [OMIM:615286]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37 [OMIM:615493]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38 [OMIM:615516]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 [OMIM:615541]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40 [OMIM:615599]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41 [OMIM:615637]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42 [OMIM:615802]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43 [OMIM:615817]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44 [OMIM:615942]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45 [OMIM:615979]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 [OMIM:616116]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47 [OMIM:616193]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48 [OMIM:616269]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49 [OMIM:616281]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50 [OMIM:616460]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51 [OMIM:616739]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52 [OMIM:616887]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53 [OMIM:616917]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54 [OMIM:617028]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55 [OMIM:617051]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56 [OMIM:617125]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57 [OMIM:617188]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58 [OMIM:617270]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59 [OMIM:617323]	(0|0)	(0|0|0)
- 1:	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60 [OMIM:617432]	(0|0)	(0|0|0)
- 1:	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION [OMIM:152950]	(0|0)	(0|0|0)
- 1:	MOMES Syndrome [MESH:C564660]	(0|0)	(0|0|0)
- 1:	MORM syndrome [MESH:C536984]	(0|0)	(0|0|0)
- 1:	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY [OMIM:617404]	(0|0)	(0|0|0)
- 1:	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 [OMIM:613155]	(0|0)	(0|0|0)
- 1:	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14 [OMIM:615351]	(0|0)	(0|0|0)
- 1:	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 [OMIM:613156]	(0|0)	(0|0|0)
- 1:	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 [OMIM:613151]	(0|0)	(0|0|0)
- 1:	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 [OMIM:608840]	(0|0)	(0|0|0)
- 1:	Macrogyria, pseudobulbar palsy and mental retardation [MESH:C537722]	(0|0)	(0|0|0)
- 1:	Macrosomia obesity macrocephaly ocular abnormalities [MESH:C535812]	(0|0)	(0|0|0)
- 1:	Male pseudohermaphroditism-mental retardation syndrome, Verloes type [MESH:C535693]	(0|0)	(0|0|0)
- 1:	Mandibulofacial Dysostosis with Mental Deficiency [MESH:C565420]	(0|0)	(0|0|0)
- 1:	Marfanoid Mental Retardation Syndrome, Autosomal [MESH:C565410]	(0|0)	(0|0|0)
- 1:	Marinesco-Sjogren-like syndrome (MSLS) [MESH:C535913]	(0|0)	(0|0|0)
- 1:	Martin-Probst Deafness-Mental Retardation Syndrome [MESH:C564495]	(0|0)	(0|0|0)
- 1:	Martsolf syndrome [MESH:C536028]	(0|0)	(0|0|0)
- 1:	McDonough syndrome [MESH:C538158]	(0|0)	(0|0|0)
- 1:	Mental Retardation associated with Psoriasis [MESH:C564107]	(0|0)	(0|0|0)
- 1:	Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature [MESH:C563810]	(0|0)	(0|0|0)
- 1:	Mental Retardation with Spastic Paraplegia [MESH:C564099]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Dominant 1 [MESH:C566947]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Dominant 3 [MESH:C567241]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Dominant 4 [MESH:C567240]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Dominant 5 [MESH:C567234]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 1 [MESH:C565406]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 10 [MESH:C567013]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 11 [MESH:C567012]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 12 [MESH:C567019]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 13 [MESH:C567714]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 2 [MESH:C564404]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 3 [MESH:C563929]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 4 [MESH:C567008]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 5 [MESH:C567018]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 6 [MESH:C567017]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 7 [MESH:C567016]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 8 [MESH:C567015]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Autosomal Recessive 9 [MESH:C567014]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Buenos Aires Type [MESH:C563095]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Fra12a Type [MESH:C566980]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities [MESH:C567209]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Microcephaly, Epilepsy, And Coarse Face [MESH:C563342]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism [MESH:C565246]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration [MESH:C566429]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations [MESH:C565248]	(0|0)	(0|0|0)
- 1:	Mental Retardation, Skeletal Dysplasia, and Abducens Palsy [MESH:C564101]	(0|0)	(0|0|0)
- 1:	Mental Retardation, X-Linked, Syndromic 12 [MESH:C564106]	(0|0)	(0|0|0)
- 1:	Mental Retardation, X-Linked, Syndromic, Christianson Type [MESH:C567484]	(0|0)	(0|0|0)
- 1:	Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476]	(0|0)	(0|0|0)
- 1:	Mental Retardation, X-Linked, Syndromic, Zdhhc9-Related [MESH:C567586]	(0|0)	(0|0|0)
- 1:	Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485]	(0|0)	(0|0|0)
- 1:	Mental Retardation, X-Linked, Znf711-Related [MESH:C567583]	(0|0)	(0|0|0)
- 1:	Mental and Growth Retardation with Amblyopia [MESH:C563591]	(0|0)	(0|0|0)
- 1:	Mental retardation Mietens Weber type [MESH:C537444]	(0|0)	(0|0|0)
- 1:	Mental retardation Smith Fineman Myers type [MESH:C537445]	(0|0)	(0|0|0)
- 1:	Mental retardation Wolff type [MESH:C537448]	(0|0)	(0|0|0)
- 1:	Mental retardation spasticity ectrodactyly [MESH:C537446]	(0|0)	(0|0|0)
- 1:	Mental retardation syndrome, Belgian type [MESH:C537447]	(0|0)	(0|0|0)
- 1:	Mental retardation, keratoconus, febrile seizures, and sinoatrial block [MESH:C537452]	(0|0)	(0|0|0)
- 1:	Mental retardation, macrocephaly, short stature and craniofacial dysmorphism [MESH:C537453]	(0|0)	(0|0|0)
- 1:	Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness [MESH:C565396]	(0|0)	(0|0|0)
- 1:	Methionine Malabsorption Syndrome [MESH:C562682]	(0|0)	(0|0|0)
- 1:	Microcephalic primordial dwarfism Toriello type [MESH:C537321]	(0|0)	(0|0|0)
- 1:	Microcephaly cervical spine fusion anomalies [MESH:C537325]	(0|0)	(0|0|0)
- 1:	Microcephaly deafness syndrome [MESH:C537326]	(0|0)	(0|0|0)
- 1:	Microcephaly seizures mental retardation heart disorders [MESH:C537544]	(0|0)	(0|0|0)
- 1:	Microcephaly sparse hair mental retardation seizures [MESH:C537545]	(0|0)	(0|0|0)
- 1:	Microcephaly with Mental Retardation and Digital Anomalies [MESH:C567101]	(0|0)	(0|0|0)
- 1:	Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation [MESH:C566361]	(0|0)	(0|0|0)
- 1:	Microcephaly, Macrotia, And Mental Retardation [MESH:C566525]	(0|0)	(0|0|0)
- 1:	Microcephaly, corpus callosum dysgenesis and cleft lip-palate [MESH:C537547]	(0|0)	(0|0|0)
- 1:	Microphthalmia and mental deficiency [MESH:C537462]	(0|0)	(0|0|0)
- 1:	Mohr-Tranebjaerg syndrome [MESH:C535808]	(0|0)	(0|0|0)
- 1:	Mollica Pavone Antener syndrome [MESH:C535809]	(0|0)	(0|0|0)
- 1:	Morillo-Cucci Passarge syndrome [MESH:C536983]	(0|0)	(0|0|0)
- 1:	Mowat-Wilson syndrome [MESH:C536990]	(0|0)	(0|0|0)
- 1:	Muscular Dystrophy, Congenital, Type 1D [MESH:C563844]	(0|0)	(0|0|0)
- 1:	Muscular Dystrophy, Congenital, associated with Calf Hypertrophy, Microcephaly, and Severe Mental Re [MESH:C565506]	(0|0)	(0|0|0)
- 1:	Muscular Dystrophy, Congenital, plus Mental Retardation [MESH:C565505]	(0|0)	(0|0|0)
- 1:	Myotonia with Skeletal Abnormalities and Mental Retardation [MESH:C564967]	(0|0)	(0|0|0)
- 1:	N syndrome [MESH:C536108]	(0|0)	(0|0|0)
- 1:	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT [OMIM:614254]	(0|0)	(0|0|0)
- 1:	NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS [OMIM:615075]	(0|0)	(0|0|0)
- 1:	NF1 Microduplication Syndrome [MESH:C567173]	(0|0)	(0|0|0)
- 1:	Nakamura Osame syndrome [MESH:C538335]	(0|0)	(0|0|0)
- 1:	Neuhauser syndrome [MESH:C536143]	(0|0)	(0|0|0)
- 1:	Neurofaciodigitorenal syndrome [MESH:C537388]	(0|0)	(0|0|0)
- 1:	Neurologic Disease, Infantile Multisystem, with Osseous Fragility [MESH:C564954]	(0|0)	(0|0|0)
- 1:	Nicolaides Baraitser syndrome [MESH:C536116]	(0|0)	(0|0|0)
- 1:	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME [OMIM:617062]	(0|0)	(0|0|0)
- 1:	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES [OMIM:616732]	(0|0)	(0|0|0)
- 1:	Oculodigitoesophagoduodenal syndrome [MESH:C537734]	(0|0)	(0|0|0)
- 1:	Oliver Syndrome [MESH:C564931]	(0|0)	(0|0|0)
- 1:	Oliver-McFarlane syndrome [MESH:C536554]	(0|0)	(0|0|0)
- 1:	Onychotrichodysplasia and neutropenia [MESH:C537752]	(0|0)	(0|0|0)
- 1:	Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency [MESH:C563498]	(0|0)	(0|0|0)
- 1:	Opitz trigonocephaly syndrome [MESH:C537418]	(0|0)	(0|0|0)
- 1:	Osteolysis syndrome recessive [MESH:C536052]	(0|0)	(0|0|0)
- 1:	PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS [OMIM:600176]	(0|0)	(0|0|0)
- 1:	PHOSPHOSERINE PHOSPHATASE DEFICIENCY [OMIM:614023]	(0|0)	(0|0|0)
- 1:	Palant cleft palate syndrome [MESH:C538102]	(0|0)	(0|0|0)
- 1:	Pallister W syndrome [MESH:C538106]	(0|0)	(0|0|0)
- 1:	Parastremmatic dwarfism [MESH:C537172]	(0|0)	(0|0|0)
- 1:	Parkinsonism, early onset with mental retardation [MESH:C537179]	(0|0)	(0|0|0)
- 1:	Pashayan syndrome [MESH:C536303]	(0|0)	(0|0|0)
- 1:	Patella hypoplasia mental retardation [MESH:C536308]	(0|0)	(0|0|0)
- 1:	Pavone Fiumara Rizzo syndrome [MESH:C536313]	(0|0)	(0|0|0)
- 1:	Perisylvian syndrome [MESH:C536658]	(0|0)	(0|0|0)
- 1:	Perniola Krajewska Carnevale syndrome [MESH:C536660]	(0|0)	(0|0|0)
- 1:	Pfeiffer Kapferer syndrome [MESH:C537887]	(0|0)	(0|0|0)
- 1:	Pfeiffer Mayer syndrome [MESH:C537888]	(0|0)	(0|0|0)
- 1:	Pfeiffer Tietze Welte syndrome [MESH:C537891]	(0|0)	(0|0|0)
- 1:	Pilotto syndrome [MESH:C537400]	(0|0)	(0|0|0)
- 1:	Piussan Lenaerts Mathieu syndrome [MESH:C537511]	(0|0)	(0|0|0)
- 1:	Primrose syndrome [MESH:C536420]	(0|0)	(0|0|0)
- 1:	Prolonged Bleeding Time, Brachydactyly, and Mental Retardation [MESH:C564207]	(0|0)	(0|0|0)
- 1:	Proud Syndrome [MESH:C563110]	(0|0)	(0|0|0)
- 1:	Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness [MESH:C562894]	(0|0)	(0|0|0)
- 1:	Pseudoaminopterin syndrome [MESH:C535823]	(0|0)	(0|0|0)
- 1:	Pseudouridinuria and Mental Defect [MESH:C564864]	(0|0)	(0|0|0)
- 1:	Pterygium colli mental retardation digital anomalies [MESH:C535831]	(0|0)	(0|0|0)
- 1:	Qazi Markouizos syndrome [MESH:C536259]	(0|0)	(0|0|0)
- 1:	Radioulnar synostosis retinal pigment abnormalities [MESH:C536270]	(0|0)	(0|0|0)
- 1:	Ramon Syndrome [MESH:C535285]	(0|0)	(0|0|0)
- 1:	Ramos Arroyo Clark syndrome [MESH:C535286]	(0|0)	(0|0|0)
- 1:	Reardon Wilson Cavanagh syndrome [MESH:C535295]	(0|0)	(0|0|0)
- 1:	Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038]	(0|0)	(0|0|0)
- 1:	Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism [MESH:C564841]	(0|0)	(0|0|0)
- 1:	Richards-Rundle syndrome [MESH:C535674]	(0|0)	(0|0|0)
- 1:	Robin Sequence with Distinctive Facial Appearance and Brachydactyly [MESH:C563880]	(0|0)	(0|0|0)
- 1:	Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant [MESH:C563392]	(0|0)	(0|0|0)
- 1:	Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked [MESH:C564467]	(0|0)	(0|0|0)
- 1:	Rud Syndrome [MESH:C535878]	(0|0)	(0|0|0)
- 1:	Ruzicka Goerz Anton syndrome [MESH:C537192]	(0|0)	(0|0|0)
- 1:	SCARF syndrome [MESH:C536625]	(0|0)	(0|0|0)
- 1:	SECKEL SYNDROME 4 [OMIM:613676]	(0|0)	(0|0|0)
- 1:	SUPERNUMERARY DER(22)t(8 [OMIM:613700]	(0|0)	(0|0|0)
- 1:	Sammartino De Crecchio Syndrome [MESH:C537229]	(0|0)	(0|0|0)
- 1:	Sao Paulo MCA-MR Syndrome [MESH:C563119]	(0|0)	(0|0|0)
- 1:	Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511]	(0|0)	(0|0|0)
- 1:	Schinzel-Giedion syndrome [MESH:C536632]	(0|0)	(0|0|0)
- 1:	Schofer Beetz Bohl syndrome [MESH:C535949]	(0|0)	(0|0|0)
- 1:	Scholte syndrome [MESH:C536638]	(0|0)	(0|0|0)
- 1:	Schrander-Stumpel Theunissen Hulsmans syndrome [MESH:C536639]	(0|0)	(0|0|0)
- 1:	Sclerosing bone dysplasia mental retardation [MESH:C537523]	(0|0)	(0|0|0)
- 1:	Scott Bryant Graham syndrome [MESH:C537528]	(0|0)	(0|0|0)
- 1:	SeSAME syndrome [MESH:C557674]	(0|0)	(0|0|0)
- 1:	Seckel Syndrome 3 [MESH:C563881]	(0|0)	(0|0|0)
- 1:	Seemanova Lesny syndrome [MESH:C537536]	(0|0)	(0|0|0)
- 1:	Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atyp [MESH:C566989]	(0|0)	(0|0|0)
- 1:	Simpson-Golabi-Behmel syndrome [MESH:C537340]	(0|0)	(0|0|0)
- 1:	Singh Chhaparwal Dhanda syndrome [MESH:C537341]	(0|0)	(0|0|0)
- 1:	Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306]	(0|0)	(0|0|0)
- 1:	Spastic Paraplegia 18, Autosomal Recessive [MESH:C567628]	(0|0)	(0|0|0)
- 1:	Spastic Paraplegia 32, Autosomal Recessive [MESH:C566983]	(0|0)	(0|0|0)
- 1:	Spastic Paraplegia, Ataxia, And Mental Retardation [MESH:C564378]	(0|0)	(0|0|0)
- 1:	Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy [MESH:C566682]	(0|0)	(0|0|0)
- 1:	Spastic Paresis, Glaucoma, and Mental Retardation [MESH:C564809]	(0|0)	(0|0|0)
- 1:	Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation [MESH:C564808]	(0|0)	(0|0|0)
- 1:	Spastic diplegia infantile type [MESH:C537481]	(0|0)	(0|0|0)
- 1:	Spastic paraplegia 14, autosomal recessive [MESH:C537486]	(0|0)	(0|0|0)
- 1:	Spastic paraplegia epilepsy mental retardation [MESH:C536869]	(0|0)	(0|0|0)
- 1:	Spinal Muscular Atrophy with Mental Retardation [MESH:C564807]	(0|0)	(0|0|0)
- 1:	Spinal Muscular Atrophy with Microcephaly and Mental Subnormality [MESH:C564806]	(0|0)	(0|0|0)
- 1:	Spondyloepimetaphyseal dysplasia, Genevieve type [MESH:C535785]	(0|0)	(0|0|0)
- 1:	Spondyloepiphyseal Dysplasia Tarda with Mental Retardation [MESH:C564796]	(0|0)	(0|0|0)
- 1:	Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Reta [MESH:C566515]	(0|0)	(0|0|0)
- 1:	Stevenson-Carey Syndrome [MESH:C567446]	(0|0)	(0|0|0)
- 1:	Sucrosuria, Hiatus Hernia and Mental Retardation [MESH:C564792]	(0|0)	(0|0|0)
- 1:	TAKENOUCHI-KOSAKI SYNDROME [OMIM:616737]	(0|0)	(0|0|0)
- 1:	TATTON-BROWN-RAHMAN SYNDROME [OMIM:615879]	(0|0)	(0|0|0)
- 1:	TENORIO SYNDROME [OMIM:616260]	(0|0)	(0|0|0)
- 1:	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE [OMIM:601675]	(0|0)	(0|0|0)
- 1:	Tamari Goodman syndrome [MESH:C536896]	(0|0)	(0|0|0)
- 1:	Temple-Baraitser Syndrome [MESH:C567516]	(0|0)	(0|0|0)
- 1:	Temtamy preaxial brachydactyly syndrome [MESH:C536958]	(0|0)	(0|0|0)
- 1:	Tetrasomy X [MESH:C536502]	(0|0)	(0|0|0)
- 1:	Tonoki syndrome [MESH:C536967]	(0|0)	(0|0|0)
- 1:	Trichodental syndrome [MESH:C536551]	(0|0)	(0|0|0)
- 1:	Trisomy 13 Syndrome [MESH:D000073839]	(0|0)	(0|0|0)
- 1:	Tryptophanuria With Dwarfism [MESH:C562658]	(0|0)	(0|0|0)
- 1:	Tsukahara Syndrome [MESH:C566376]	(0|0)	(0|0|0)
- 1:	Ulna hypoplasia with mental retardation [MESH:C536934]	(0|0)	(0|0|0)
- 1:	Ulnar Hypoplasia with Mental Retardation [MESH:C564757]	(0|0)	(0|0|0)
- 1:	Upton Young syndrome [MESH:C536473]	(0|0)	(0|0|0)
- 1:	Van Bogaert-Hozay syndrome [MESH:C536526]	(0|0)	(0|0|0)
- 1:	Van Den Bosch Syndrome [MESH:C563129]	(0|0)	(0|0|0)
- 1:	Van Maldergem Wetzburger Verloes syndrome [MESH:C536530]	(0|0)	(0|0|0)
- 1:	Vasquez Hurst Sotos syndrome [MESH:C536533]	(0|0)	(0|0|0)
- 1:	Verloes Gillerot Fryns syndrome [MESH:C536539]	(0|0)	(0|0|0)
- 1:	Viljoen Kallis Voges syndrome [MESH:C536349]	(0|0)	(0|0|0)
- 1:	Vitiligo, Progressive, with Mental Retardation and Urethral Duplication [MESH:C564739]	(0|0)	(0|0|0)
- 1:	Volcke Soekarman syndrome [MESH:C537718]	(0|0)	(0|0|0)
- 1:	WIEDEMANN-STEINER SYNDROME [OMIM:605130]	(0|0)	(0|0|0)
- 1:	Walker Dyson syndrome [MESH:C536568]	(0|0)	(0|0|0)
- 1:	Warburg Sjo Fledelius syndrome [MESH:C536681]	(0|0)	(0|0|0)
- 1:	Warburton Anyane Yeboa syndrome [MESH:C536682]	(0|0)	(0|0|0)
- 1:	Wiedemann Grosse Dibbern syndrome [MESH:C536704]	(0|0)	(0|0|0)
- 1:	Wiedemann Oldigs Oppermann syndrome [MESH:C536705]	(0|0)	(0|0|0)
- 1:	Winship Viljoen Leary syndrome [MESH:C536711]	(0|0)	(0|0|0)
- 1:	Woodhouse Sakati syndrome [MESH:C536742]	(0|0)	(0|0|0)
- 1:	Worster Drought syndrome [MESH:C536747]	(0|0)	(0|0|0)
- 1:	XIA-GIBBS SYNDROME [OMIM:615829]	(0|0)	(0|0|0)
- 1:	Yorifuji Okuno syndrome [MESH:C536714]	(0|0)	(0|0|0)
- 1:	Young Hughes syndrome [MESH:C536715]	(0|0)	(0|0|0)
- 1:	Young Simpson syndrome [MESH:C536717]	(0|0)	(0|0|0)
- 1:	ZTTK SYNDROME [OMIM:617140]	(0|0)	(0|0|0)
- 1:	Zazam Sheriff Phillips syndrome [MESH:C536723]	(0|0)	(0|0|0)
- 1:	Zechi-Ceide Syndrome [MESH:C567865]	(0|0)	(0|0|0)
- 1:	Zerres Rietschel Majewski syndrome [MESH:C536724]	(0|0)	(0|0|0)
- 1:	Zlotogora-Ogur syndrome [MESH:C536726]	(0|0)	(0|0|0)
- 1:	Zunich neuroectodermal syndrome [MESH:C536729]	(0|0)	(0|0|0)

Superfamily

Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
BRK domain-like	0.0009874	DIRECT
Thioredoxin-like	0.5312	INHERITED FROM: Down Syndrome

Family

Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
BRK domain-like	0.0006004	DIRECT
Bromodomain	0.0008622	DIRECT

Supra-domain (Single|Duplex|Triple)

Supra-domain (Single)

Highlighted in gray are those with FDR>0.001

Supra-domain (Single)	FDR (all)	Annotation (direct or inherited)
BRK domain-like	0.0006389	DIRECT
Thioredoxin-like	0.4974	INHERITED FROM: Down Syndrome

Supra-domain (Duplex) in N- to C-terminal order

Highlighted in gray are those with FDR>0.001

Supra-domain (Duplex) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
53822,53850 53822 - Periplasmic binding protein-like I 53850 - Periplasmic binding protein-like II	0.0006389	DIRECT