MYO1F

myosin IF
OMIM: 601480, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red MYO1F in Mendeliome


Version 1.4044

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • ClinGen
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497
Tags
  • disputed

Red MYO1F in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.315

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497
Tags
  • disputed

Red MYO1F in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.315

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497
Tags
  • disputed

Red MYO1F in Additional findings_Paediatric


Level 2: Screening
Version 0.279

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

Red MYO1F in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 1.147

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