congenital aphakia

Summary
Synonym
  • APHAKIA, CONGENITAL PRIMARY
  • Congenital absence of lens
Super Class
lens disease physical disorder
External Links
Disease Ontology
DOID:11367
Mondo Disease Ontology
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
4051 CYP4F3 cytochrome P450 family 4 subfamily F member 3
50863 NTM neurotrimin
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q9P121 Neurotrimin

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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