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DO Term : nephronophthisis 13 [DOID:0111121] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14.

synonyms:
614377,
OMIM:614377,
NPHP13

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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