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Familial parathyroid adenoma

1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

5 OMIM references -
4 associated genes
11 signs/symptoms

Familial parathyroid adenoma

Nephroblastoma

CDC73	(UniProt - OMIM)		DIS3L2	(UniProt - OMIM)
MEN1	(UniProt - OMIM)		H19	(OMIM)
			POU6F2	(UniProt - OMIM)
			WT1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MEN1 MEN1	(0.63) (0.63)	H19 WT1

Citations in the biomedical literature:

Familial parathyroid adenoma		Nephroblastoma
	Synonym(s): (no synonyms)		Synonym(s): - Renal embryonic tumor - Wilms tumor

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: any age Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 5 OMIM references - 1 MeSH reference: D009396

Nephroblastoma
	Very frequent - Acute abdominal pain / colic - Kidney / renal neoplasm / tumor / carcinoma / cancer - Neoplasms / tumors Occasional - Aniridia / iris hypoplasia - Chronic arterial hypertension - Fever / chilling - Hematuria / microhematuria - Hepatic / liver neoplasm / tumor / carcinoma / cancer - Lung / bronchopulmonary neoplasm / tumor / carcinoma / cancer - Lymphadenopathy / polyadenopathies - Weight loss / loss of appetite / break in weight curve / general health alteration
Familial parathyroid adenoma
(no data available)