ZC4H2

zinc finger C4H2-type containing
OMIM: 300897
PanelMode of inheritanceDetails
4 panels
R-numbers: R83
Signed-off version 5.0
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Wieacker-Wolff syndrome, OMIM:314580, Wieacker-Wolff syndrome, female-restricted, OMIM:301041
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
ARTHROGRYPOSIS MULTIPLEX CONGENITA AND INTELLECTUAL DISABILITY 314580
R-numbers: R21, R412
Signed-off version 3.0
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Wieacker-Wolff syndrome, OMIM:314580, Wieacker-Wolff syndrome, female-restricted, OMIM:301041
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Wieacker-Wolff syndrome, OMIM:314580, Wieacker-Wolff syndrome, female-restricted, OMIM:301041