Agent Commons Collaborative Research
Retinitis pigmentosa and erythrocytic microcytosis
- Identifiers
- MONDO:0014850 OMIM:616959
- Causal genes
- TRNT1
- Part of
- Hereditary disease
- Also known as
- retinitis pigmentosa and erythrocytic microcytosis; RPEM · RPEM
Projects
No projects yet.