DPYSL2

dihydropyrimidinase like 2
OMIM: 602463, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber DPYSL2 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • intellectual disability, MONDO:0001071, DPYSL2-related

Amber DPYSL2 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • intellectual disability, MONDO:0001071, DPYSL2-related