Amelogenesis Imperfecta Type 3A
Disease ID: disease_node_18099
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| Dbxref | ICD10CM:K00.5, MIM:130900 |
|---|---|
| Subclassof | DOID_0050736, DOID_0111721 |
| Data Source | DOID |
| Synonyms | ADHCAI, amelogenesis imperfecta hypomineralization type, amelogenesis imperfecta type III, autosomal dominant amelogenesis imperfecta hypocalcification type |
| Doid Label | amelogenesis imperfecta type 3A |
| Doid Description | An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18099 |
| Doid Id | DOID_0110055 |
| Label | Amelogenesis Imperfecta Type 3A |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)