MYO1C

myosin IC
OMIM: 606538, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red MYO1C in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Sensorineural hearing loss

Red MYO1C in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Sensorineural hearing loss