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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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