Arthrogryposis Multiplex Congenita-4
Disease ID: disease_node_20567
Connections displayed (default: 10).
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| Dbxref | MIM:618766 |
|---|---|
| Subclassof | DOID_0080954 |
| Data Source | DOID |
| Synonyms | Zain syndrome |
| Doid Label | arthrogryposis multiplex congenita-4 |
| Doid Description | An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20567 |
| Doid Id | DOID_0080980 |
| Label | Arthrogryposis Multiplex Congenita-4 |
- Outgoing r'ship
SUBCLASS_OFto/from Arthrogryposis Multiplex Congenita(ID:disease_node_20565) (Disease)