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Zollinger-Ellison syndrome
1 associated gene
54 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Multiple endocrine neoplasia type 1
Autosomal dominant nonsyndromic intellectual deficit
Precursor T-cell acute lymphoblastic leukemia
Precursor B-cell acute lymphoblastic leukemia
Anaplastic ependymoma
Pulverulent cataract
Alexander disease type I
Alexander disease type II
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Craniopharyngioma
Desmoid tumor
Fanconi anemia
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Common variable immunodeficiency
Estrogen resistance syndrome
Autosomal agammaglobulinemia
Burkitt lymphoma
Fuchs endothelial corneal dystrophy
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
46,XY partial gonadal dysgenesis
Acute basophilic leukemia
Cerebellar ataxia - hypogonadism
Denys-Drash syndrome
Desmoplastic small round cell tumor
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Frasier syndrome
Meacham syndrome
Nephroblastoma
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
WAGR syndrome
X-linked dystonia-parkinsonism
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Methylmalonic acidemia with homocystinuria, type cblX
X-linked non-syndromic intellectual deficit
Acrodysostosis
Acrodysostosis with multiple hormone resistance
Carney complex
Familial atrial myxoma
Primary pigmented nodular adrenocortical disease
Synonym(s):
- Gastrinoma
Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare oncologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: sporadic
External references:
No OMIM references
2 MeSH references: D015043 / D015408
Gene symbol UniProt reference OMIM reference
MEN1 O00255613733
No signs/symptoms info available.