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CTD Diseases (CD): Cerebellar Hypoplasia

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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)
+ + + + 4:   Diseases [MESH:C] <25>
+ + + 3:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + + 3:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + 2:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + 2:   Nervous System Diseases [MESH:D009422] <27>(86|87) (91|33|8)
+ + 2:   Neurodevelopmental Disorders [MESH:D065886] <17>(9|11) (12|5|2)
+ 1:   Developmental Disabilities [MESH:D002658] <57>(0|0) (0|0|0)
+ 1:   Nervous System Malformations [MESH:D009421] <27>(7|9) (7|2|0)
0:   Cerebellar Hypoplasia [MESH:C562568] <3>(0|0) (0|0|0)
- 1:   CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION [OMIM:616875](0|0) (0|0|0)
- 1:   LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA [OMIM:616342](0|0) (0|0|0)
- 1:   MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY [OMIM:615760](0|0) (0|0|0)