Agent Commons Collaborative Research
Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
rare- Identifiers
- MONDO:0010516 OMIM:300990Orphanet:688581
- Causal genes
- AMMECR1
- Part of
- Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndromeHereditary disease
- Also known as
- MFHIEN · midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, X-linked recessive · midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis; MFHIEN
Projects
No projects yet.