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Succinyl-coa:3-oxoacid coa transferase deficiency
Succinyl-coa:3-oxoacid coa transferase deficiency
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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
succinyl CoA:3-oxoacid CoA transferase deficiency
MONDO_0009492
OXCT1
Unknown
10964512
11757586
1405472
21296660
23281106
23420214
25778941
27604308
31073471
33596448
8751852
9671268
Open Targets
Valine, leucine and isoleucine degradation
Butanoate metabolism
Metabolic pathways
Utilization of Ketone Bodies
+1 more
SUCCINYL-COA-3-KETOACID-COA transferase deficiency
MONDO_0009492
OXCT1
Unknown
10964512
9671268
1405472
23281106
Open Targets
Valine, leucine and isoleucine degradation
Butanoate metabolism
Metabolic pathways
Utilization of Ketone Bodies
+1 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
0
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Succinyl-coa:3-oxoacid coa transferase deficiency.
3
View disease cluster →
Osteoporosis
1 shared gene
OXCT1
Related via 1 shared gene including OXCT1.
Mitochondrial disease
1 shared gene
OXCT1
Related via 1 shared gene including OXCT1.
Bipolar disorder
1 shared gene
OXCT1
Related via 1 shared gene including OXCT1.
1
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