Wolfram syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WOLFRAM SYNDROME
3463C0043207MONDO:0018105
CISD2 Unknown — CTD, ClinGen, Disgenet, Orphanet —
ND1 Unknown
19483677 24874954 29760529 29892088 31171569 9618163
Disgenet
WOLFRAM SYNDROME 2
C1858028
CISD3 Unknown — Disgenet —
PCGF2 Unknown
12754709 12913071 15056606 16151413 16806192 18249014 21446023 21602428 24705017 24823368 25690803 27341211 34434372
Disgenet
SLC9B1 Unknown — Disgenet
All6 Causal2 Unknown5
Related Diseases Diseases that share the most curated genes with Wolfram syndrome.
5 View disease cluster →
Turnpenny-fry syndrome 2 shared genesPCGF2, CISD3 Related via 2 shared genes including PCGF2, CISD3. Other specified diabetes mellitus with unspecified complications 1 shared geneWFS1 Related via 1 shared gene including WFS1. Wolfram-like syndrome 1 shared geneWFS1 Related via 1 shared gene including WFS1. Deafness, sensorineural, autosomal-mitochondrial type 1 shared geneND1 Related via 1 shared gene including ND1. Deafness, aminoglycoside-induced 1 shared geneND1 Related via 1 shared gene including ND1.