Autosomal recessive osteopetrosis 7

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

Also known as: OPTB7, TNFRSF11A osteopetrosis (disease), autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia, autosomal recessive osteopetrosis type 7, osteopetrosis (disease) caused by mutation in TNFRSF11A, osteopetrosis, autosomal recessive type 7, osteopetrosis-hypogammaglobulinemia syndrome, osteopetrosis autosomal recessive 7

0 clinical trials for this condition and its sub-types.