Seckel Syndrome 9
Disease ID: disease_node_20375
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| Dbxref | MIM:616777 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL9 |
| Doid Label | Seckel syndrome 9 |
| Doid Description | A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21. |
| Disease Node Id | disease_node_20375 |
| Doid Id | DOID_0070005 |
| Label | Seckel Syndrome 9 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)