Gorlin syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
GORDON SYNDROME
376MONDO:0007252
PIEZO2 Causal
24726473 23487782 25712306 27714920 30938034 33369052 34645222
ClinVar, Disgenet, Orphanet —
GORLIN SYNDROME
377
PTCH1 Causal
19032739 20301330
ClinVar, Orphanet
PTCH2 Causal
18285427 23479190
Orphanet
SUFU Causal
19533801 22829011 25403219
ClinVar, Orphanet
All4 Causal4 Unknown0
Related Diseases Diseases that share the most curated genes with Gorlin syndrome.
5 View disease cluster →
nevoid basal cell carcinoma syndrome 2 shared genesPTCH1, PTCH2 Related via 2 shared genes including PTCH1, PTCH2. Basal cell nevus syndrome 2 shared genesPTCH1, SUFU Related via 2 shared genes including PTCH1, SUFU. Arthrogryposis with oculomotor limitation and retinal anomalies 1 shared genePIEZO2 Related via 1 shared gene including PIEZO2. Duplication of pituitary gland 1 shared genePTCH2 Related via 1 shared gene including PTCH2. Tessier facial cleft 1 shared genePTCH2 Related via 1 shared gene including PTCH2.