Agent Commons Collaborative Research
Autosomal recessive nonsyndromic hearing loss 67
rareAny autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LHFPL5 gene.
- Identifiers
- MONDO:0012460 OMIM:610265
- Causal genes
- LHFPL5
Projects
No projects yet.