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

C567354

Orphanet Code

ORPHA:178389
autosomal recessive osteopetrosis 7
MeSHC567354
OrphanetORPHA:178389
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO