| Metadata | |
|---|---|
| ID | DOID:0080980 |
| Name | arthrogryposis multiplex congenita-4 |
| Definition | An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23. https://pubmed.ncbi.nlm.nih.gov/31960134/ |
| Xrefs | |
| Synonyms |
Zain syndrome [EXACT] |
| Parent Relationships |