Seckel Syndrome 6
Disease ID: disease_node_20374
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| Dbxref | MIM:614728 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL6 |
| Doid Label | Seckel syndrome 6 |
| Doid Description | A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22. |
| Disease Node Id | disease_node_20374 |
| Doid Id | DOID_0070006 |
| Label | Seckel Syndrome 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)