Seckel Syndrome 4
Disease ID: disease_node_20371
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| Dbxref | MIM:613676 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL4 |
| Doid Label | Seckel syndrome 4 |
| Doid Description | A Seckel syndrome that has_material_basis_in homozygous mutation in the CENPJ gene on chromosome 13q12. |
| Disease Node Id | disease_node_20371 |
| Doid Id | DOID_0070010 |
| Label | Seckel Syndrome 4 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)