ERBB4

erb-b2 receptor tyrosine kinase 4
OMIM: 600543, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber ERBB4 in Neurodegenerative disorders - adult onset


Version 2.57
Latest signed off version: v2.56 (16 Dec 2021)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • NHS GMS
  • Yorkshire and North East GLH
Phenotypes
  • Amyotrophic lateral sclerosis 19 OMIM:615515
  • amyotrophic lateral sclerosis type 19 MONDO:0014223
Tags
  • Q2_21_rating

Red ERBB4 in Amyotrophic lateral sclerosis/motor neuron disease

Level 3: Neurodegenerative disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.34

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Amyotrophic lateral sclerosis 19, 615515

Red ERBB4 in Hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 2.159
Latest signed off version: v2.158 (29 Jun 2021)

review Not set
Sources
  • Expert

Amber ERBB4 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.1002
Latest signed off version: v3.1001 (16 Dec 2021)

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • intellectual disability MONDO:0001071
    Tags
    • Q2_21_NHS_review
    • Q2_21_rating