OBO ID: DOID:0080981
Term Name: arthrogryposis multiplex congenita-5 Search Ontology:
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 arthrogryposis multiplex congenita-5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TOR1A Arthrogryposis multiplex congenita 5
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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