DisGeNET - a database of gene-disease associations

Source: INFERRED

Gene: FOXRED1 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1838979
Disease:	MITOCHONDRIAL COMPLEX I DEFICIENCY

MITOCHONDRIAL COMPLEX I DEFICIENCY

disease

0.600

strong

1.000

1998

2016

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C4748791
Disease:	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19

MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19

disease

0.600

None

1.000

2010

2015

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0023264
Disease:	Leigh Disease

Leigh Disease

disease

0.420

moderate

1.000

2010

2019

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0013421
Disease:	Dystonia

Dystonia

phenotype

0.400

limited

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0557874
Disease:	Global developmental delay

Global developmental delay

disease

0.110

None

1.000

2019

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0432072
Disease:	Dysmorphic features

Dysmorphic features

disease

0.100

None

1.000

2010

2016

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1963184
Disease:	Nystagmus, CTCAE 3.0

Nystagmus, CTCAE 3.0

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1277241
Disease:	Delayed myelination

Delayed myelination

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1384666
Disease:	hearing impairment

hearing impairment

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1445953
Disease:	Poor eye contact

Poor eye contact

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1531647
Disease:	Cerebral ventriculomegaly

Cerebral ventriculomegaly

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1836038
Disease:	Poor head control

Poor head control

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1836440
Disease:	Increased serum lactate

Increased serum lactate

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1167918
Disease:	Increased CSF lactate

Increased CSF lactate

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0740279
Disease:	Cerebellar atrophy

Cerebellar atrophy

disease

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0035334
Disease:	Retinitis Pigmentosa

Retinitis Pigmentosa

disease

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0554970
Disease:	Pallor of optic disc

Pallor of optic disc

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0456909
Disease:	Blindness

Blindness

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0393525
Disease:	Progressive cerebellar ataxia

Progressive cerebellar ataxia

disease

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0270612
Disease:	Leukoencephalopathy

Leukoencephalopathy

group

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0232466
Disease:	Feeding difficulties

Feeding difficulties

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C0002871
Disease:	Anemia

Anemia

disease

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C1839603
Disease:	Proximal tubulopathy

Proximal tubulopathy

phenotype

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C4721453
Disease:	Peripheral Nervous System Diseases

Peripheral Nervous System Diseases

group

0.100

None

Entrez Id:	55572
Gene Symbol:	FOXRED1

FOXRED1

FAD dependent oxidoreductase domain containing 1

0.633

0.462

2.0E-16

CUI:	C4554036
Disease:	Nystagmus, CTCAE 5.0

Nystagmus, CTCAE 5.0

phenotype

0.100

None