autosomal recessive osteopetrosis 2 (Q32145046)
Jump to navigation
Jump to search
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the TNFSF11 gene on chromosome 13q14
- OPTB2
- mild autosomal recessive form osteopetrosis
- osteoclast-poor osteopetrosis
- Osteopetrosis autosomal recessive 2
- Osteopetrosis osteoclast-poor
- Osteopetrosis, Autosomal Recessive type 2
- OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2
- Osteopetrosis, Osteoclast-Poor
- OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2
- Osteopetrosis, Mild Autosomal Recessive Form
- autosomal recessive osteopetrosis type 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive osteopetrosis 2 |
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the TNFSF11 gene on chromosome 13q14 |
|
Statements
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
2 references
1 reference
1 reference
1 reference