PanelApp (test)
  1. Genes and Genomic Entities
  2. SARDH

SARDH

sarcosine dehydrogenase
OMIM: 604455, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber SARDH in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert Review Amber
  • Literature
  • Victorian Clinical Genetics Services
Phenotypes
  • Sarcosinemia MIM#268900
  • Disorders of serine, glycine or glycerate metabolism

Amber SARDH in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 1.46

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Sarcosinemia MIM#268900
    • Disorders of serine, glycine or glycerate metabolism

    Red SARDH in Aminoacidopathy


    Level 2: Metabolic disorders
    Version 1.128

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • ClinGen
    Phenotypes
    • sarcosinemia MONDO:0010008