PHD finger protein 21A
OMIM: 608325
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Potocki-Shaffer syndrome, 601224, PSS, Intellectual disability, Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures, 618725