OBO ID: DOID:0080978
Term Name: arthrogryposis multiplex congenita-1 Search Ontology:
Synonyms:
Definition: An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the LGI4 gene on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/28318499/
References:
Ontology: Human Disease   ( DOID:0080978 )
OTHER arthrogryposis multiplex congenita-1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LGI4 Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None