WormBase Tree Display for DO_term: DOID:0060884
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DOID:0060884 | Name | renal hypomagnesemia 6 | |||
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Status | Valid | ||||
Definition | A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24. | ||||
Synonym | Exact | HOMG6 | |||
Parent | Is_a | DOID:0060879 | |||
DB_info | Database | OMIM | disease | 613882 | |
Attribute_of | Gene_by_orthology | WBGene00016343 | |||
WBGene00016879 | |||||
WBGene00019869 |