Amelogenesis Imperfecta Type 1A
Disease ID: disease_node_18106
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| Dbxref | ICD10CM:K00.5, MIM:104530 |
|---|---|
| Subclassof | DOID_0050736, DOID_2187 |
| Data Source | DOID |
| Synonyms | AI1A, amelogenesis imperfecta hypoplastic type IA, amelogenesis imperfecta type IA |
| Doid Label | amelogenesis imperfecta type 1A |
| Doid Description | An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18106 |
| Doid Id | DOID_0110054 |
| Label | Amelogenesis Imperfecta Type 1A |
- Outgoing r'ship
SUBCLASS_OFto/from Amelogenesis Imperfecta(ID:disease_node_1139) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)