CHRM1

cholinergic receptor muscarinic 1
OMIM: 118510, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber CHRM1 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neurodevelopmental delay
  • intellectual disability
  • autism

Red CHRM1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert Review
    • Expert Review Amber
    • Literature
    Phenotypes
    • Neurodevelopmental disorder
    • intellectual disability
    • autism
    • epilepsy

    Amber CHRM1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Neurodevelopmental delay
    • intellectual disability
    • autism