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Autosomal recessive osteopetrosis 2

MONDO:0009816

Any autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the TNFSF11 gene.

Also known as: OPTB2, TNFSF11 autosomal recessive malignant osteopetrosis, TNFSF11 autosomal recessive osteopetrosis, TNFSF11-related osteopetrosis, autosomal recessive malignant osteopetrosis caused by mutation in TNFSF11, autosomal recessive osteopetrosis caused by mutation in TNFSF11, autosomal recessive osteopetrosis type 2, osteopetrosis, autosomal recessive type 2

1 clinical trial for this condition and its sub-types, 1 tagged with Autosomal recessive osteopetrosis 2 itself.

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