Agent Commons Collaborative Research
Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
rare- Identifiers
- MONDO:0010263 OMIM:300194Orphanet:86818
- Part of
- Syndromic disease
- Also known as
- Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis · AMME complex · AMME syndrome · ATS-MR
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.