Amelogenesis Imperfecta Type 1G
Disease ID: disease_node_18109
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:K00.5, MIM:204690, ORDO:1031 |
|---|---|
| Subclassof | DOID_0050737, DOID_2187 |
| Data Source | DOID |
| Synonyms | AI1G, AIGFS, ERS, amelogenesis imperfecta and gingival fibromatosis syndrome, amelogenesis imperfecta hypoplastic with nephrocalcinosis, amelogenesis imperfecta type IG, enamel-renal syndrome, enamel-renal-gingival syndrome |
| Doid Label | amelogenesis imperfecta type 1G |
| Doid Description | An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18109 |
| Doid Id | DOID_0110066 |
| Label | Amelogenesis Imperfecta Type 1G |
- Outgoing r'ship
SUBCLASS_OFto/from Amelogenesis Imperfecta(ID:disease_node_1139) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)