Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception. 27923065

2016

Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 gene. 24628582

2015

Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR Genetic mapping and exome sequencing identify variants associated with five novel diseases. 22279524

2012

Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1. 21267618

2011

Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR Mutations in FLVCR1 cause posterior column ataxia and retinitis pigmentosa. 21070897

2010

Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.110 GeneticVariation CLINVAR An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa. 9409377

1997