autosomal recessive osteopetrosis 7 (Q32145086)
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osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TNFRSF11A gene on chromosome 18q21
- osteopetrosis-hypogammaglobulinemia syndrome
- autosomal recessive osteopetrosis type 7
- OPTB7
- autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
- osteoclast-poor osteopetrosis with hypogammaglobulinemia
- Osteopetrosis, Autosomal Recessive type 7
- Osteopetrosis autosomal recessive 7
- OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7
- Osteopetrosis osteoclast-poor with hypogammaglobulinemia
- OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7
- Osteopetrosis, Osteoclast-Poor, With Hypogammaglobulinemia
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive osteopetrosis 7 |
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TNFRSF11A gene on chromosome 18q21 |
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