Fanconi syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FANCONI SYNDROME
C0015624MESH:D005198
EHHADH Unknown — CTD, Disgenet
GATM Unknown — CTD, Disgenet
GPX3 Unknown
9851889
CTD, Disgenet
SLC2A2 Unknown
11810292
CTD, Disgenet
SLC34A1 Unknown — CTD, Disgenet
PRIMARY FANCONI RENOTUBULAR SYNDROME
3337
EHHADH Unknown
24401050
Orphanet
GATM Unknown
29654216
Orphanet
NDUFAF6 Unknown
27466185
Orphanet
SLC34A1 Unknown
20335586
Orphanet
PRIMARY FANCONI SYNDROME
MONDO:0007600
EHHADH Unknown
24401050
GWAS catalog
GATM Unknown
29654216
GWAS catalog
NDUFAF6 Unknown
27466185
CTD
SLC34A1 Unknown
20335586
Disgenet
All6 Causal0 Unknown6
Related Diseases Diseases that share the most curated genes with Fanconi syndrome.
5 View disease cluster →
De toni-debre-fanconi syndrome 4 shared genesGATM, EHHADH, NDUFAF6, SLC34A1 Related via 4 shared genes including GATM, EHHADH, NDUFAF6. Fanconi renotubular syndrome 4 shared genesGATM, EHHADH, NDUFAF6, SLC34A1 Related via 4 shared genes including GATM, EHHADH, NDUFAF6. Agat deficiency 1 shared geneGATM Related via 1 shared gene including GATM. Arginine-glycine amidinotransferase deficiency 1 shared geneGATM Related via 1 shared gene including GATM. Bifunctional enzyme deficiency 1 shared geneEHHADH Related via 1 shared gene including EHHADH.