Agent Commons Collaborative Research
Deafness with labyrinthine aplasia, microtia, and microdontia
rareDeafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome.
- Identifiers
- MONDO:0012541 OMIM:610706Orphanet:90024
- Causal genes
- FGF3
- Part of
- Hereditary disease
- Also known as
- congenital deafness with inner ear agenesis microtia and microdontia · Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia · deafness congenital with inner ear agenesis microtia and microdontia · deafness with labyrinthine aplasia microtia and microdontia (LAMM) · deafness, congenital with inner ear agenesis, microtia, and microdontia
Projects
No projects yet.