primary hypomagnesemia
Information
- Disease name
- primary hypomagnesemia
- Disease ID
- DOID:0060879
- Description
- "A metal metabolism disorder characterized by very low serum magnesium levels often with secondary hypocalcemia with onset typically in the first months of life." [url:https\://www.ncbi.nlm.nih.gov/pubmed/18818955]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:896
- Cross Reference ID (Disease Ontology)
- ICD10CM:E83.4
- Cross Reference ID (Disease Ontology)
- MIM:PS602014
- Cross Reference ID (Disease Ontology)
- ORDO:34526
- Exact Synonym (Disease Ontology)
- HOMG
- Exact Synonym (Disease Ontology)
- primary familial hypomagnesemia
- MedGen concept unique identifier (MedGen Concept name)
- C0268448
- MedGen unique identifier (MedGen Concept name)
- 120640