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5 OMIM references -
4 associated genes
11 signs/symptoms
PROTEIN INTERACTIONS: 2
2 OMIM references -
2 associated genes
No signs/symptoms info
Nephroblastoma
Familial isolated hyperparathyroidism

DIS3L2 CDC73
H19 MEN1
POU6F2
WT1


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
DIS3L2 H19 POU6F2 WT1
Familial isolated hyperparathyroidism
CDC73 MEN1



Nephroblastoma
Familial isolated hyperparathyroidism

Synonym(s):
- Renal embryonic tumor
- Wilms tumor

Synonym(s):
- FIHPT

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:
2 OMIM references -
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 isolated hyperparathyroidism

(no data available)