Warburg micro syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WARBURG MICRO SYNDROME
C5442005MONDO:0016649
RAB18 Unknown
21473985 23420520 24764192 25779931 26879639
ClinGen, Disgenet, GWAS catalog
RAB3GAP2 Unknown
16532399 20967465 23420520 24891604 32376645 32740904
ClinGen, Disgenet
TBC1D20 Unknown
24239381
Disgenet, GWAS catalog
WARBURG MICRO SYNDROME 1
C1838625
RAB18 Unknown — Disgenet
RAB3GAP2 Unknown — Disgenet
TBC1D20 Unknown — Disgenet
WARBURG SJO FLEDELIUS SYNDROME
MESH:C536681
RAB18 Unknown
21473985 26063829 29300443
CTD, ClinGen
RAB3GAP1 Unknown
10465117 15216543 15696165 20512159 29675078
CTD, ClinGen
RAB3GAP2 Unknown — CTD, ClinGen
TBC1D20 Unknown
24239381
CTD
All4 Causal4 Unknown4
Related Diseases Diseases that share the most curated genes with Warburg micro syndrome.
5 View disease cluster →
Congenital malformation syndromes predominantly affecting facial appearance 4 shared genesRAB18, RAB3GAP1, RAB3GAP2, TBC1D20 Related via 4 shared genes including RAB18, RAB3GAP1, RAB3GAP2. Apert syndrome 4 shared genesRAB18, RAB3GAP1, RAB3GAP2, TBC1D20 Related via 4 shared genes including RAB18, RAB3GAP1, RAB3GAP2. Cryptophthalmos syndrome 4 shared genesRAB18, RAB3GAP1, RAB3GAP2, TBC1D20 Related via 4 shared genes including RAB18, RAB3GAP1, RAB3GAP2. Cyclocephaly 4 shared genesRAB18, RAB3GAP1, RAB3GAP2, TBC1D20 Related via 4 shared genes including RAB18, RAB3GAP1, RAB3GAP2. Cataract-intellectual disability-hypogonadism syndrome 2 shared genesRAB3GAP1, RAB3GAP2 Related via 2 shared genes including RAB3GAP1, RAB3GAP2.