AMFR

autocrine motility factor receptor
OMIM: 603243, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green AMFR in Mendeliome


Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spastic paraplegia 89, autosomal recessive, MIM# 620379
  • Inborn error of immunity, MONDO:0003778, AMFR-related

Red AMFR in Disorders of immune dysregulation


Level 2: Immunological disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • Inborn error of immunity, MONDO:0003778, AMFR-related

Green AMFR in Hereditary Spastic Paraplegia


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spastic paraplegia 89, autosomal recessive, MIM# 620379