Disease #02345 (HYPOC1 (hypocalcemia, autosomal dominant, Bartter syndrome incl. (HYPOC-1)), OMIM:601198)
| Official abbreviation |
HYPOC1 |
| Name |
hypocalcemia, autosomal dominant, Bartter syndrome incl. (HYPOC-1) |
| OMIM ID |
601198 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
105 |
| Phenotype entries for this disease |
88 |
| Associated with 1 gene |
CASR |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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