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DO Term : Warburg micro syndrome 1 [DOID:0110716] 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 RAB3GAP1 gene on chromosome 2q21.
  • synonyms:
  • WARBM1,
  • ICD10CM:Q87.0,
  • OMIM:600118,
  • Micro Syndrome 1,
  • 600118
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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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