Search Ontology:
Human Disease

congenital hydrocephalus 3

Term ID
DOID:0070684
Synonyms
Definition
A congenital hydrocephalus that has_material_basis_in homozygous mutation in the WDR81 gene on chromosome 17p13. https://pubmed.ncbi.nlm.nih.gov/28556411/
References
Ontology
Human Disease   ( DOID:0070684 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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