cataract 32 multiple types

Summary
Synonym
  • CTRCT32
Definition
A cataract that has_material_basis_in mutation in the region 14q22-q23.
Super Class
autosomal dominant disease cataract
External Links
Disease Ontology
DOID:0110227
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 21 - 27 of 27 in total
Gene ID Gene Symbol Description Source
26503 SLC17A5 solute carrier family 17 member 5
51084 CRYL1 crystallin lambda 1
51763 INPP5K inositol polyphosphate-5-phosphatase K
55750 AGK acylglycerol kinase
81031 SLC2A10 solute carrier family 2 member 10
653509 SFTPA1 surfactant protein A1
729238 SFTPA2 surfactant protein A2

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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: August 19, 2024