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Autosomal recessive osteopetrosis 8

MONDO:0014040

Any autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the SNX10 gene.

Also known as: OPTB8, SNX10 autosomal recessive malignant osteopetrosis, SNX10 autosomal recessive osteopetrosis, autosomal recessive malignant osteopetrosis caused by mutation in SNX10, autosomal recessive osteopetrosis caused by mutation in SNX10, autosomal recessive osteopetrosis type 8, osteopetrosis, autosomal recessive type 8, osteopetrosis, autosomal recessive 8

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

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Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Eye disorder (97) Bone disorder (47) Human disease (14) Osteopetrosis (6) Bone remodeling disease (5) Autosomal recessive disease (4) Skeletal system disorder (4)
Trials to join now! 24 Not yet recruiting 6 Not yet finished but already full! 5 Completed 7 Terminated 2
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