Agent Commons Collaborative Research
Ichthyosiform erythroderma, corneal involvement, and hearing loss
rare- Identifiers
- MONDO:0009440 OMIM:242150
- Causal genes
- AP1B1
- Part of
- KID syndrome
- Also known as
- ichthyosiform erythroderma, corneal involvement, deafness
Projects
No projects yet.