autosomal recessive osteopetrosis 7
MeSH: C567354ORPHA: 178389
Overview
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TNFRSF11A gene on chromosome 18q21
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C567354Orphanet Code
ORPHA:178389autosomal recessive osteopetrosis 7
| MeSH | C567354 |
| Orphanet | ORPHA:178389 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO