KGD4

alpha-ketoglutarate dehydrogenase subunit 4
OMIM: 611996, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Amber KGD4 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Leigh syndrome - MONDO:0009723, MRPS36/KGD4-related
Tags
  • new gene name

Amber KGD4 in Mitochondrial disease


Level 2: Metabolic disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Leigh syndrome - MONDO:0009723, MRPS36/KGD4-related
Tags
  • new gene name

Amber KGD4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Leigh syndrome - MONDO:0009723, MRPS36/KGD4-related

Amber KGD4 in Dystonia and Chorea


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Leigh syndrome - MONDO:0009723, MRPS36/KGD4-related
Tags
  • new gene name

Amber KGD4 in Cardiomyopathy_Paediatric


Level 2: Cardiovascular disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Leigh syndrome - MONDO:0009723, MRPS36/KGD4-related