Amelogenesis Imperfecta Type 3B
Disease ID: disease_node_18100
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| Dbxref | MIM:617607 |
|---|---|
| Subclassof | DOID_0050736, DOID_0111721 |
| Data Source | DOID |
| Doid Label | amelogenesis imperfecta type 3B |
| Doid Description | An amelogenesis imperfecta type 3 that is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places and that has_material_basis_in heterozygous mutation in the amelotin gene. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18100 |
| Doid Id | DOID_0080243 |
| Label | Amelogenesis Imperfecta Type 3B |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)