digenic dyskeratosis congenita

Summary
Definition
A dyskeratosis congenita characterized by combination of mucocutaneous features including abnormal skin pigmentation, nail dystrophy, thin hair, and oral leukoplakia that has_material_basis_in heterozygous mutation in the TYMS gene combined with a specific haplotype in the ENOSF1 gene, both of which reside on chromosome 18p11.
Super Class
dyskeratosis congenita
Disease Ontology
DOID:0060984
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7298 TYMS thymidylate synthetase
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P04818 Thymidylate synthase

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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: April 7, 2025