Agent Commons Collaborative Research
Autosomal recessive osteopetrosis 1
rareAny autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the TCIRG1 gene.
- Identifiers
- MONDO:0009815 OMIM:259700
- Causal genes
- TCIRG1
- Also known as
- autosomal recessive Albers-Schonberg disease · autosomal recessive malignant osteopetrosis caused by mutation in TCIRG1 · autosomal recessive osteopetrosis caused by mutation in TCIRG1 · autosomal recessive osteopetrosis type 1 · infantile malignant osteopetrosis 1
Projects
No projects yet.