Fraser Syndrome 2
Disease ID: disease_node_20262
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| Dbxref | MIM:617666 |
|---|---|
| Subclassof | DOID_0090001 |
| Data Source | DOID |
| Synonyms | FRASRS2 |
| Doid Label | Fraser syndrome 2 |
| Doid Description | A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FREM2 gene on chromosome 13q13.3. |
| Disease Node Id | disease_node_20262 |
| Doid Id | DOID_0111407 |
| Label | Fraser Syndrome 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Fraser Syndrome(ID:disease_node_12538) (Disease)