糖酵解紊乱

Disorder of glycolysis

ORPHA:308459疾病组

相关基因 27来自下位疾病

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来，「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因	名称	来源条目
ABCC8	ATP binding cassette subfamily C member 8	ORPHA:552
ALDOA	aldolase, fructose-bisphosphate A	ORPHA:57
APPL1	adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1	ORPHA:552
BLK	BLK proto-oncogene, Src family tyrosine kinase	ORPHA:552
CEL	carboxyl ester lipase	ORPHA:552
ENO3	enolase 3	ORPHA:99849
GCK	glucokinase	ORPHA:79299
GPI	glucose-6-phosphate isomerase	ORPHA:712
HK1	hexokinase 1	ORPHA:90031
HNF1A	HNF1 homeobox A	ORPHA:552
HNF1B	HNF1 homeobox B	ORPHA:93111
HNF4A	hepatocyte nuclear factor 4 alpha	ORPHA:552
INS	insulin	ORPHA:552
KCNJ11	potassium inwardly rectifying channel subfamily J member 11	ORPHA:552
KLF11	KLF transcription factor 11	ORPHA:552
LDHA	lactate dehydrogenase A	ORPHA:284426
LDHB	lactate dehydrogenase B	ORPHA:284435
NARS2	asparaginyl-tRNA synthetase 2, mitochondrial	ORPHA:79134
NEUROD1	neuronal differentiation 1	ORPHA:552
PAX4	paired box 4	ORPHA:552
PDX1	pancreatic and duodenal homeobox 1	ORPHA:552
PFKM	phosphofructokinase, muscle	ORPHA:371
PGAM2	phosphoglycerate mutase 2	ORPHA:97234
PGK1	phosphoglycerate kinase 1	ORPHA:713
PKLR	pyruvate kinase L/R	ORPHA:766
STAT3	signal transducer and activator of transcription 3	ORPHA:99885
TPI1	triosephosphate isomerase 1	ORPHA:868

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