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CTD Diseases (CD): Timothy syndrome

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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)
+ + + + + + 6:   Diseases [MESH:C] <25>
+ + + + + 5:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + + 5:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ + + + + 5:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + + + 4:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + + 4:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
+ + + + 4:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + + 4:   Neurodevelopmental Disorders [MESH:D065886] <17>(9|11) (12|5|2)
+ + + + 4:   Cardiovascular Diseases [MESH:D002318] <5>(37|36) (38|13|9)
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + 3:   Musculoskeletal Abnormalities [MESH:D009139] <30>(9|16) (12|4|4)
+ + + 3:   Dysostoses [MESH:D004413] <23>(1|2) (1|1|1)
+ + + 3:   Heart Diseases [MESH:D006331] <31>(16|16) (19|5|4)
+ + + 3:   Child Development Disorders, Pervasive [MESH:D002659] <2>(4|6) (7|1|0)
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Cardiovascular Abnormalities [MESH:D018376] <6>(2|4) (3|1|2)
+ + 2:   Limb Deformities, Congenital [MESH:D017880] <114>(3|4) (3|1|2)
+ + 2:   Arrhythmias, Cardiac [MESH:D001145] <27>(2|2) (2|0|0)
+ + 2:   Heart Defects, Congenital [MESH:D006330] <142>(2|4) (3|0|2)
+ + 2:   Cardiac Conduction System Disease [MESH:D000075224] <12>(1|1) (1|0|0)
+ + 2:   Synostosis [MESH:D013580] <29>(1|2) (1|1|1)
+ + 2:   Autism Spectrum Disorder [MESH:D000067877] <2>(4|6) (7|1|0)
+ 1:   Autistic Disorder [MESH:D001321] <7>(3|5) (5|1|0)
+ 1:   Long QT Syndrome [MESH:D008133] <20>(1|1) (1|0|0)
+ 1:   Syndactyly [MESH:D013576] <57>(0|1) (0|1|1)
0:   Timothy syndrome [MESH:C536962](0|0) (0|0|0)