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DO Term : Warburg micro syndrome 3 [DOID:0110718] 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 RAB18 gene on chromosome 10p12.
  • synonyms:
  • Micro Syndrome 3,
  • ICD10CM:Q87.0,
  • 614222,
  • WARBM3,
  • OMIM:614222
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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