NME3

NME/NM23 nucleoside diphosphate kinase 3
OMIM: 601817, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NME3 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Hypotonia
  • Neurodegeneration
  • Abnormal mitochondrial dynamics

Red NME3 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.927

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Hypotonia
    • Neurodegeneration
    • Abnormal mitochondrial dynamics