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Linear skin defects with multiple congenital anomalies 2
Linear skin defects with multiple congenital anomalies 2
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Subtype of:
Linear skin defects with multiple congenital anomalies
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(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
Linear skin defects with multiple congenital anomalies 2
MONDO_0010672
COX7B
Causal
33670341
23122588
Open Targets
Oxidative phosphorylation
Metabolic pathways
Cardiac muscle contraction
Thermogenesis
Non-alcoholic fatty liver disease
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
TP53 Regulates Metabolic Genes
Respiratory electron transport
+12 more
Linear Skin Defects with Multiple Congenital Anomalies 2, LSDMCA2
MONDO_0010672
COX7B
Unknown
23122588
Open Targets
Oxidative phosphorylation
Metabolic pathways
Cardiac muscle contraction
Thermogenesis
Non-alcoholic fatty liver disease
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
TP53 Regulates Metabolic Genes
Respiratory electron transport
+12 more
All
1
Causal
1
Unknown
1
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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 Linear skin defects with multiple congenital anomalies 2.
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No strongly related diseases found yet for Linear skin defects with multiple congenital anomalies 2.
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