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DO Term : Galloway-Mowat syndrome 1 [DOID:0060364] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.

synonyms:
nephrosis-neuronal dysmigration syndrome,
autosomal recessive spinocerebellar ataxia 5,
microcephaly, hiatal hernia and nephrotic syndrome,
OMIM:251300,
Galloway syndrome,
251300,
nephrosis-microcephaly syndrome,
SCAR5

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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