1. Genes and Genomic Entities
  2. SARDH

SARDH

sarcosine dehydrogenase
OMIM: 604455, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SARDH in Undiagnosed metabolic disorders

Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.617

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Sarcosinaemia (Disorders of serine, glycine or glycerate metabolism)
  • [Sarcosinemia] 268900
Red SARDH in Likely inborn error of metabolism - targeted testing not possible


Version 4.137
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • London North GLH
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • [Sarcosinemia] 268900
    • Sarcosinaemia (Disorders of serine, glycine or glycerate metabolism)