Cytoscape Web
Click node...

Familial parathyroid adenoma
1 OMIM reference -
2 associated genes
76 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated hyperparathyroidism
Hyperparathyroidism - jaw tumor syndrome
Multiple endocrine neoplasia type 1
Parathyroid carcinoma
Zollinger-Ellison syndrome
Autosomal dominant nonsyndromic intellectual deficit
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Fuchs endothelial corneal dystrophy
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Estrogen resistance syndrome
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
Fanconi anemia
Common variable immunodeficiency
Acute necrotizing encephalopathy of childhood
Familial acute necrotizing encephalopathy
Inflammatory myofibroblastic tumor
Autosomal agammaglobulinemia
Burkitt lymphoma
46,XY partial gonadal dysgenesis
Acute basophilic leukemia
Anophthalmia / microphthalmia - esophageal atresia
Cerebellar ataxia - hypogonadism
Colobomatous microphthalmia
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
Familial short QT syndrome
Frasier syndrome
ICF syndrome
Infantile Refsum disease
Isolated anophthalmia - microphthalmia
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Meacham syndrome
Metachondromatosis
Neonatal adrenoleukodystrophy
Nephroblastoma
Noonan syndrome
Periventricular nodular heterotopia
Pilocytic astrocytoma
Romano-Ward syndrome
Septo-optic dysplasia
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
WAGR syndrome
X-linked dystonia-parkinsonism
Zellweger syndrome
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Gliosarcoma
Intellectual deficit, X-linked, Nascimento type
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):
(no synonyms)
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CDC73 Q6P1J9607393
MEN1 O00255613733
No signs/symptoms info available.