ZC4H2

zinc finger C4H2-type containing
OMIM: 300897, ClinGen, DECIPHER

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Green ZC4H2 in Arthrogryposis Level 2: Neurology and neurodevelopmental disorders Version 1.1 Component of the following Super Panels: Neuromuscular Superpanel	2 reviews	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Wieacker-Wolff syndrome (MIM#314580)
Green ZC4H2 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.405	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Wieacker-Wolff syndrome, MIM# 314580
Green ZC4H2 in Mendeliome Version 1.3795	2 reviews	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Wieacker-Wolff syndrome, MIM# 314580
Green ZC4H2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.497	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Genetic Health Queensland Phenotypes Wieacker-Wolff syndrome, MIM# 314580
Green ZC4H2 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.111	0 reviews	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Wieacker-Wolff syndrome, 314580 (3)
Green ZC4H2 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Expert Review Phenotypes Wieacker-Wolff syndrome, MIM# 314580
Green ZC4H2 in Fetal anomalies Version 1.481	2 reviews	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Wieacker-Wolff syndrome, OMIM#314580 Wieacker-Wolff syndrome, female-restricted, OMIM#301041
Green ZC4H2 in Prepair 1000+ Level 2: Screening Version 2.15	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Mackenzie's Mission Phenotypes Wieacker-Wolff syndrome MIM#314580