Lacrimoauriculodentodigital Syndrome 3
Disease ID: disease_node_20092
Connections displayed (default: 10).
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| Dbxref | MIM:620193 |
|---|---|
| Subclassof | DOID_0050736, DOID_0081370 |
| Data Source | DOID |
| Synonyms | Lacrimo-auriculo-dento-digital syndrome 3 |
| Doid Label | lacrimoauriculodentodigital syndrome 3 |
| Doid Description | A LADD syndrome that is characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary systems, cup-shaped ears, hearing loss, and dental and digital anomalies and that has_material_basis_in heterozygous mutation in the FGF10 gene on chromosome 5p12. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20092 |
| Doid Id | DOID_0081372 |
| Label | Lacrimoauriculodentodigital Syndrome 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Ladd Syndrome(ID:disease_node_20093) (Disease)