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DO Term : Galloway-Mowat syndrome 5 [DOID:0080247] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the TPRKB gene on chromosome 2p13.
  • synonyms:
  • 617731,
  • OMIM:617731
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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