MIEF1

mitochondrial elongation factor 1
OMIM: 615497, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red MIEF1 in Mendeliome


Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Optic atrophy 14 (MIM#620550)

Red MIEF1 in Optic Atrophy


Level 2: Ophthalmological disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Optic atrophy 14 (MIM#620550)

Red MIEF1 in Mitochondrial disease


Level 2: Metabolic disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Optic atrophy 14 (MIM#620550)