autosomal dominant hypocalcemia 1
Information
- Disease name
- autosomal dominant hypocalcemia 1
- Disease ID
- DOID:0090107
- Description
- "An autosomal dominant hypocalcemia disease that has_material_basis_in heterozygous mutation in the calcium sensing receptor gene (CASR) on chromosome 3q21." [url:https\://ghr.nlm.nih.gov/condition/autosomal-dominant-hypocalcemia, url:https\://www.omim.org/entry/601198]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0090109
- Cross Reference ID (Disease Ontology)
- MIM:601198
- Exact Synonym (Disease Ontology)
- HYPOC1