1. Genes and Genomic Entities
  2. MARVELD2

MARVELD2

MARVEL domain containing 2
OMIM: 610572, Gene2Phenotype

2 panels

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

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.4

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


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

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