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Primary sclerosing cholangitis
2 OMIM references -
3 associated genes
44 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant nonsyndromic intellectual deficit
Fuchs endothelial corneal dystrophy
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Precursor T-cell acute lymphoblastic leukemia
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Catecholaminergic polymorphic ventricular tachycardia
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Haddad syndrome
Ondine syndrome
Papillary or follicular thyroid carcinoma
Hyperparathyroidism - jaw tumor syndrome
Parathyroid carcinoma
Miller-Dieker syndrome
Multiple endocrine neoplasia type 1
Zollinger-Ellison syndrome
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute promyelocytic leukemia
Amyotrophic lateral sclerosis
Autosomal agammaglobulinemia
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Myxofibrosarcoma
Myxoid / round cell liposarcoma
Neuroblastoma
Precursor B-cell acute lymphoblastic leukemia
Young adult-onset Parkinsonism
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Lethal acantholytic epidermolysis bullosa
Naxos disease
Alpha-1-antichymotrypsin deficiency
Congenital prekallikrein deficiency
MODY syndrome
Synonym(s):
- PSC
Classification (Orphanet):
- Rare hepatic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
2 OMIM references -
1 MeSH reference: C536419
Gene symbol UniProt reference OMIM reference
GPR35 Q9HC97602646
MST1 P26927142408
TCF4 P15884602272
No signs/symptoms info available.