(Q32145059)
English
autosomal recessive osteopetrosis 4
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the CLCN7 gene on chromosome 16p13
- OPTB4
- infantile malignant osteopetrosis 2
- autosomal recessive osteopetrosis type 4
- OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4
- Osteopetrosis infantile malignant 2
- Osteopetrosis, Autosomal Recessive type 4
- Osteopetrosis, Infantile Malignant 2
- OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4; OPTB4
- Osteopetrosis autosomal recessive 4
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