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Autosomal recessive osteopetrosis 7

rare

Any autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the TNFRS11A gene.

Identifiers
MONDO:0012859 OMIM:612301Orphanet:178389
Causal genes
TNFRSF11A
Part of
Autosomal recessive osteopetrosisImmune system disorder
Also known as
autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia · autosomal recessive osteopetrosis type 7 · OPTB7 · osteopetrosis (disease) caused by mutation in TNFRSF11A · osteopetrosis autosomal recessive 7

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