EYA4

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green EYA4 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 10, MIM# 601316 Cardiomyopathy, dilated, 1J, MIM# 605362
Green EYA4 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.210	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal dominant 10, MIM# 601316
Amber EYA4 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.196	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber London South GLH South West GLH NHS GMS Phenotypes Cardiomyopathy, dilated, 1J, MIM# 605362
Green EYA4 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Deafness, autosomal dominant
Red EYA4 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category A gene Phenotypes Deafness, autosomal dominant 10, MIM# 601316

5 panels