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 1.1

review Unknown
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Sporadic Meniere disease
  • Deafness, autosomal recessive 49 610153

Green MARVELD2 in Hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 2.200
Latest signed off version: v2.5 (13 Feb 2020)

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 1.84

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