AMPD1

adenosine monophosphate deaminase 1
OMIM: 102770, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red AMPD1 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Myopathy due to myoadenylate deaminase deficiency (MIM#615511)
Tags
  • disputed

Red AMPD1 in Rhabdomyolysis and Metabolic Myopathy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Royal Melbourne Hospital
Phenotypes
  • Myopathy due to myoadenylate deaminase deficiency 615511
  • Rhabdomyolysis
Tags
  • disputed

Red AMPD1 in Additional findings_Paediatric


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Adenosine monophosphate deaminase deficiency

Red AMPD1 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Adenosine monophosphate deaminase deficiency

Red AMPD1 in Nucleotide metabolism disorders


Level 2: Metabolic disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • adenosine monophosphate deaminase deficiency MONDO:0013028