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| Term | renal hypomagnesemia 4 | ID (Ontology) | DOID:0060882 (Human Disease) |
| Definition | 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. | ||
| Also Known As | "HOMG4" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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metal metabolism disorder |__primary hypomagnesemia |__renal hypomagnesemia 4 1 rec. |
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| Is a | primary hypomagnesemia | ||
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ICD10CM:E83.4 MIM:611718 ORDO:34527 |
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