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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Alpers-Huttenlocher syndrome +   
cerebral lipidosis 
hydrocephalus +   
A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head. (DO)
leukodystrophy +   
neuroaxonal dystrophy +   
senile degeneration of brain 

Synonyms
Exact Synonyms: Cerebral Ventriculomegaly ;   Congenital Hydrocephalus ;   HYC1 ;   aqueductal stenoses ;   aqueductal stenosis ;   cerebral ventriculomegalies ;   fetal cerebral ventriculomegalies ;   fetal cerebral ventriculomegaly ;   hydrocephalus ex vacuo ;   hydrocephalus ex-vacuos ;   hydrocephalus, X-linked ;   hydrocephaly ;   nonsyndromic hydrocephalus, autosomal recessive ;   nonsyndromic hydrocephalus, autosomal recessive 1 ;   post traumatic hydrocephalus ;   ventriculomegaly
Narrow Synonyms: SEVERE HYDROCEPHALUS
Primary IDs: MESH:D006849
Alternate IDs: OMIM:236600 ;   OMIM:236635
Xrefs: GARD:6682 ;   ICD10CM:G91 ;   NCI:C3111 ;   NCI:C98876 ;   OMIM:PS236600 ;   ORDO:2182 ;   ORDO:2185
Definition Sources: http://en.wikipedia.org/wiki/Hydrocephalus "DO" "DO", http://ghr.nlm.nih.gov/glossary=hydrocephalus "DO" "DO", http://www.mayoclinic.org/diseases-conditions/hydrocephalus/basics/definition/con-20030706?_ga=1.124310025.2017809229.1415219956 "DO" "DO"

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