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Sjogren-larsson syndrome
Sjogren-larsson syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
SJOGREN-LARSSON SYNDROME
270200
816
C0037231
MESH:D016111
MONDO:0010031
ALDH3A2
Unknown
16837225
25641190
CTD
,
ClinVar
,
Disgenet
,
GenCC
,
HPO
,
Orphanet
Glycolysis / Gluconeogenesis
Ascorbate and aldarate metabolism
Fatty acid degradation
Valine, leucine and isoleucine degradation
Lysine degradation
Arginine and proline metabolism
Histidine metabolism
Tryptophan metabolism
beta-Alanine metabolism
Glycerolipid metabolism
Pyruvate metabolism
Pantothenate and CoA biosynthesis
Metabolic pathways
Biosynthesis of cofactors
Alcoholic liver disease
Sphingolipid de novo biosynthesis
Alpha-oxidation of phytanate
Class I peroxisomal membrane protein import
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
+16 more
KRT14
Unknown
—
Disgenet
Estrogen signaling pathway
Staphylococcus aureus infection
Type I hemidesmosome assembly
Keratinization
Formation of the cornified envelope
+2 more
All
2
Causal
0
Unknown
2
Select all
Clear
ClinVar
1
Orphanet
1
Disgenet
2
CTD
1
HPO
1
GWAS catalog
0
GenCC
1
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Sjogren-larsson syndrome.
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Epidermolysis bullosa simplex
1 shared gene
KRT14
Related via 1 shared gene including KRT14.
Dermatopathia pigmentosa reticularis
1 shared gene
KRT14
Related via 1 shared gene including KRT14.
Weber-cockayne syndrome
1 shared gene
KRT14
Related via 1 shared gene including KRT14.
Tongue neoplasms
1 shared gene
KRT14
Related via 1 shared gene including KRT14.
Junctional epidermolysis bullosa
1 shared gene
KRT14
Related via 1 shared gene including KRT14.
1
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