MYO3A

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green MYO3A in Mendeliome Version 1.3499	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 30, MIM# 607101 Deafness, autosomal dominant 90, MIM# 620722
Green MYO3A in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.238	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 30, MIM# 607101 Deafness, autosomal dominant 90, MIM# 620722
Green MYO3A in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Sensorineural hearing loss
Green MYO3A in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene Phenotypes Deafness, autosomal recessive 30, MIM:607101 Tags deafness

4 panels