cataract 9 multiple types

Summary
Synonym
  • CTRCT9
  • cataract 9 multiple types with or without microcornea
Definition
A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.
Super Class
autosomal dominant disease autosomal recessive disease cataract
Disease Ontology
DOID:0110266
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1409 CRYAA crystallin alpha A
Displaying 1 entry
Gene ID Gene Symbol Description Source
12954 Cryaa crystallin, alpha A
Displaying 1 entry
Gene ID Gene Symbol Description Source
24273 Cryaa crystallin, alpha A

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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