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DO Term : Warburg micro syndrome 2 [DOID:0110717] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP2 gene on chromosome 1q41.

synonyms:
614225,
ICD10CM:Q87.0,
Micro Syndrome 2,
WARBM2,
OMIM:614225

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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