OBO ID: DOID:0080978 |
Term Name: | arthrogryposis multiplex congenita-1 | Search Ontology: | |
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Synonyms: |
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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 |
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LGI4 | Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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