Seckel Syndrome 5
Disease ID: disease_node_20369
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| Dbxref | MIM:613823 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL5 |
| Doid Label | Seckel syndrome 5 |
| Doid Description | A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. |
| Disease Node Id | disease_node_20369 |
| Doid Id | DOID_0070012 |
| Label | Seckel Syndrome 5 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)