DisGeNET - a database of gene-disease associations

Movement Disorders, C0026650

Gene: ALDH5A1 ×

Source: ALL

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

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	7915
Gene Symbol:	ALDH5A1

ALDH5A1

0.100

CausalMutation

group

CLINVAR

Acute Infantile Encephalopathy as Presentation of Succinic Semialdehyde Dehydrogenase Deficiency.

27268762

2016

Entrez Id:	7915
Gene Symbol:	ALDH5A1

ALDH5A1

0.100

CausalMutation

group

CLINVAR

Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood.

26268900

2015

Entrez Id:	7915
Gene Symbol:	ALDH5A1

ALDH5A1

0.100

CausalMutation

group

CLINVAR

Succinic semialdehyde dehydrogenase deficiency: lessons from mice and men.

19172412

2009

Entrez Id:	7915
Gene Symbol:	ALDH5A1

ALDH5A1

0.100

CausalMutation

group

CLINVAR

Inherited disorders of neurotransmitters in children and adults.

16298354

2005

Entrez Id:	7915
Gene Symbol:	ALDH5A1

ALDH5A1

0.100

CausalMutation

group

CLINVAR

Clinical spectrum of succinic semialdehyde dehydrogenase deficiency.

12743223

2003

Entrez Id:	7915
Gene Symbol:	ALDH5A1

ALDH5A1

0.100

CausalMutation

group

CLINVAR

4-Hydroxybutyric aciduria.

7726383

1994