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Glutaryl-CoA dehydrogenase deficiency
Glutaryl-CoA dehydrogenase deficiency
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Subtype of:
Glutaricacidemia
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Glutaricacidemia type 1
MONDO_0009281
GCDH
Unknown
11174631
8900228
7795610
8900227
10699052
Open Targets
Fatty acid degradation
Lysine degradation
Tryptophan metabolism
Metabolic pathways
Lysine catabolism
+2 more
Glutaricaciduria, type I
MONDO_0009281
GCDH
Unknown
27604308
24816252
26316201
23884036
11174631
8900227
8900228
7795610
10699052
15985591
12473778
Open Targets
Fatty acid degradation
Lysine degradation
Tryptophan metabolism
Metabolic pathways
Lysine catabolism
+2 more
glutaryl-CoA dehydrogenase deficiency
MONDO_0009281
GCDH
Unknown
15985591
12473778
ClinGen
,
Open Targets
Fatty acid degradation
Lysine degradation
Tryptophan metabolism
Metabolic pathways
Lysine catabolism
+2 more
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
1
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Glutaryl-CoA dehydrogenase deficiency.
5
View disease cluster →
Glutaricacidemia
1 shared gene
GCDH
Related via 1 shared gene including GCDH.
Glutaric aciduria 1
1 shared gene
GCDH
Related via 1 shared gene including GCDH.
Tyrosinemia
1 shared gene
GCDH
Related via 1 shared gene including GCDH.
Congenital dyserythropoietic anemia
1 shared gene
GCDH
Related via 1 shared gene including GCDH.
Hypomyelinating leukodystrophy
1 shared gene
GCDH
Related via 1 shared gene including GCDH.
1
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