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Diseases

Carbohydrate Metabolism, Inborn Errors

carbohydrate metabolism, inborn errors

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Carbohydrate Metabolism, Inborn Errors
Standard Disease Name
carbohydrate metabolism, inborn errors
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D002239
OMIM ID
No data
UMLS ID
C0007001
HPO ID
No data

Description and Extensions

Description
MSH2017_2016_08_12:Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero.|CSP2006:condition in which there is a deviation or interruption in the processing of carbohydrates in the body, its absorption, transport, storage, and utilization.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
ABCC8
ATP binding cassette subfamily C member 8
ATP binding cassette subfamily C member 8
02
AGL
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
03
AGXT
alanine--glyoxylate and serine--pyruvate aminotransferase
alanine--glyoxylate and serine--pyruvate aminotransferase
04
ALDOB
aldolase, fructose-bisphosphate B
aldolase, fructose-bisphosphate B
06
G6PC
glucose-6-phosphatase catalytic subunit
glucose-6-phosphatase catalytic subunit