hydrocephalus

Summary

DOID:10908 - hydrocephalus

Disease Ontology Definition:A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head.

Synonyms: hydrocephalus, nonsyndromic, autosomal recessive, hydrocephalus, X-linked

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: mpdz, ccdc88c, l1cam, cfap43

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0001150 - hydrocephalus

MONDO:0001150 - hydrocephalus

MIM:

MIM:123155 - HYDROCEPHALUS, AUTOSOMAL DOMINANT; HDCPH1
MIM:236600 - HYDROCEPHALUS, CONGENITAL, 1; HYC1
MIM:236635 - HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS
MIM:307000 - HYDROCEPHALUS, CONGENITAL, X-LINKED; HYCX
MIM:615219 - HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2

MIM:123155 - HYDROCEPHALUS, AUTOSOMAL DOMINANT; HDCPH1

MIM:236600 - HYDROCEPHALUS, CONGENITAL, 1; HYC1

MIM:236635 - HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS

MIM:307000 - HYDROCEPHALUS, CONGENITAL, X-LINKED; HYCX

MIM:615219 - HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): cerebral degeneration (is_a)