ODCs

Cytoscape Web

Click node...

5 OMIM references -
4 associated genes
11 signs/symptoms

PROTEIN INTERACTIONS: 2

Familial parathyroid adenoma

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

Nephroblastoma

Familial parathyroid adenoma

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


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

Citations in the biomedical literature:

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

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

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

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

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

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)