Search Ontology:
Human Disease
arthrogryposis multiplex congenita-5
- Term ID
- DOID:0080981
- Synonyms
-
- Definition
- An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the TOR1A gene on chromosome 9q34. https://pubmed.ncbi.nlm.nih.gov/29053766/
- References
- Ontology
- Human Disease ( DOID:0080981 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations