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Standards Ontologies Notations
arthrogryposis multiplex congenita-1

Summary
Definition
An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the LGI4 gene on chromosome 19q13.
Super Class
arthrogryposis multiplex congenita
Disease Ontology
DOID:0080978
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
163175 LGI4 leucine rich repeat LGI family member 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
243914 Lgi4 leucine-rich repeat LGI family, member 4
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024