Amelogenesis Imperfecta Type 1K
Disease ID: disease_node_18117
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| Dbxref | GARD:5791, MIM:620104, ORDO:88661 |
|---|---|
| Subclassof | DOID_2187 |
| Data Source | DOID |
| Doid Label | amelogenesis imperfecta type 1K |
| Doid Description | An amelogenesis imperfecta characterized by hypoplastic enamel of all teeth that has_material_basis_in heterozygous mutation in the SP6 gene on chromosome 17q21. |
| Disease Node Id | disease_node_18117 |
| Doid Id | DOID_0060945 |
| Label | Amelogenesis Imperfecta Type 1K |
- Outgoing r'ship
SUBCLASS_OFto/from Amelogenesis Imperfecta(ID:disease_node_1139) (Disease)