Disease #00852 (HYC1 (Hydrocephalus, congenital, 1), OMIM:236600)

Official abbreviation HYC1
Name Hydrocephalus, congenital, 1
OMIM ID 236600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CCDC88C
Associated tissues -
Disease features -
Remarks -