MARVELD2

MARVEL domain containing 2
OMIM: 610572, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red MARVELD2 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.3

review Unknown
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Sporadic Meniere disease
  • Deafness, autosomal recessive 49 610153
Green MARVELD2 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.41
Latest signed off version: v4.39 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • Nonsyndromic Hearing Loss, Recessive
    • Deafness, autosomal recessive 49, 610153
    • hearing loss
    Green MARVELD2 in Severe Paediatric Disorders


    Version 1.184

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 49, 610153