Search Ontology:
Human Disease
amelogenesis imperfecta type 3A
- Term ID
- DOID:0110055
- Synonyms
-
- ADHCAI
- AI3
- amelogenesis imperfecta hypomineralization type
- amelogenesis imperfecta type III
- autosomal dominant amelogenesis imperfecta hypocalcification type
- Definition
- An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24. (2)
- References
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- ICD10CM:K00.5
- OMIM:130900
- Ontology
- Human Disease ( DOID:0110055 )
- is a type of
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