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DO Term : nephronophthisis 7 [DOID:0111116] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A nephronophthisis that has_material_basis_in homozygous mutation in the GLIS2 gene on chromosome 16p13.

synonyms:
OMIM:611498,
611498,
MESH:C566930,
NPHP7

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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