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Standards Ontologies Notations
arthrogryposis multiplex congenita-4

Summary
Synonym
  • Zain syndrome
Definition
An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23.
Super Class
arthrogryposis multiplex congenita
Disease Ontology
DOID:0080980
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
55681 SCYL2 SCY1 like pseudokinase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
213326 Scyl2 SCY1-like 2 (S. cerevisiae)
Displaying 1 entry
Gene ID Gene Symbol Description Source
852797 SCY1 Scy1p
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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