Search Ontology:
Human Disease

arthrogryposis multiplex congenita-1

Term ID
DOID:0080978
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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