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DO Term : congenital hydrocephalus 3 [DOID:0070684] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital hydrocephalus that has_material_basis_in homozygous mutation in the WDR81 gene on chromosome 17p13.

synonyms:
UMLS_CUI:C4747885,
OMIM:617967,
617967

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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