DHX37

DEAH-box helicase 37
OMIM: 617362
PanelMode of inheritanceDetails
3 panels
R-numbers: R146
Signed-off version 4.20
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
46, XY sex reversal 11, 273250
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies, OMIM:618731
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies, MIM#618731