Seckel Syndrome 10
Disease ID: disease_node_20373
Connections displayed (default: 10).
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| Dbxref | MIM:617253 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL10 |
| Doid Label | Seckel syndrome 10 |
| Doid Description | A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24. |
| Disease Node Id | disease_node_20373 |
| Doid Id | DOID_0070008 |
| Label | Seckel Syndrome 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)