DHX36

DEAH-box helicase 36
OMIM: 612767, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber DHX36 in Mendeliome


Version 2.516

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Other
  • Other
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, DHX36-related

Amber DHX36 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.125

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Other
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, DHX36-related