familial hypocalciuric hypercalcemia 1
MeSH: C537145ORPHA: 93372
Overview
familial hypocalciuric hypercalcemia that has material basis in heterozygous loss-of-function mutations in the CASR gene on chromosome 3q21
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C537145Orphanet Code
ORPHA:93372familial hypocalciuric hypercalcemia 1
| MeSH | C537145 |
| Orphanet | ORPHA:93372 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO