X-linked recessive hypoparathyroidism
MeSH: C563238ORPHA: 2239
Overview
human disease
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with X-linked recessive hypoparathyroidism, sourced from HPO and Orphanet clinical annotations.
HypocalcemiaCongenital hypoparathyroidismParathyroid agenesisHypercalciuriaHypocalcemic seizuresHyperphosphatemiaMale infertilityHypomagnesemia
Classification & Codes
MeSH Code
C563238Orphanet Code
ORPHA:2239X-linked recessive hypoparathyroidism
| MeSH | C563238 |
| Orphanet | ORPHA:2239 |
| Treatments | 0 drug(s) |
| Symptoms on record | 8 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO