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DO Term : renal hypomagnesemia 4 [DOID:0060882] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hypomagnesemia characterized by isolated hypomagnesemia due to renal loss with normal serum calcium levels and urinary calcium excretion that has_material_basis_in homozygous mutation in the EGF gene on chromosome 4q25.
  • synonyms:
  • 611718,
  • HOMG4,
  • OMIM:611718,
  • ORDO:34527,
  • ICD10CM:E83.4
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Disease

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Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents