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CTD Diseases (CD): Hypogonadism with Low-Grade Mental Deficiency and Microcephaly

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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)
+ + + + + 5:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + + 5:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Signs and Symptoms [MESH:D012816] <38>(30|33) (33|13|1)
+ + + + 4:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + + 4:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + + 4:   Nervous System Malformations [MESH:D009421] <27>(7|9) (7|2|0)
+ + + + 4:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + + 3:   Neurologic Manifestations [MESH:D009461] <26>(22|24) (25|9|1)
+ + + 3:   Endocrine System Diseases [MESH:D004700] <18>(19|28) (22|15|10)
+ + + 3:   Malformations of Cortical Development [MESH:D054220] <26>(5|5) (5|2|0)
+ + + 3:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ + 2:   Craniofacial Abnormalities [MESH:D019465] <223>(3|9) (6|1|1)
+ + 2:   Gonadal Disorders [MESH:D006058] <6>(5|4) (5|1|0)
+ + 2:   Neurobehavioral Manifestations [MESH:D019954] <10>(5|5) (5|1|0)
+ + 2:   Malformations of Cortical Development, Group I [MESH:D065703] <5>(0|1) (0|1|0)
+ + 2:   Neurodevelopmental Disorders [MESH:D065886] <17>(9|11) (12|5|2)
+ 1:   Hypogonadism [MESH:D007006] <66>(0|0) (0|0|0)
+ 1:   Intellectual Disability [MESH:D008607] <521>(2|2) (2|1|0)
+ 1:   Microcephaly [MESH:D008831] <164>(0|0) (0|0|0)
0:   Hypogonadism with Low-Grade Mental Deficiency and Microcephaly [MESH:C565482](0|0) (0|0|0)