DisGeNET - a database of gene-disease associations

Gene: SFXN4 ×

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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

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	119559
Gene Symbol:	SFXN4

SFXN4

CUI:	C3810001
Disease:	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18

0.700

GermlineCausalMutation

ORPHANET

Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4.

2013