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5 OMIM references -
4 associated genes
11 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Nephroblastoma
17q11 microdeletion syndrome

DIS3L2 NF1
H19 RNF135
POU6F2 SUZ12
WT1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WT1
(0.63)
SUZ12



Citations in the biomedical literature:


Nephroblastoma
DIS3L2 H19 POU6F2 WT1
17q11 microdeletion syndrome
NF1 RNF135 SUZ12



Nephroblastoma
17q11 microdeletion syndrome

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

Synonym(s):
- Del(17)(q11)
- Monosomy 17q11
- NF1 microdeletion syndrome
- Neurofibromatosis type 1 microdeletion syndrome

Classification (Orphanet):
- Rare genetic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare skin disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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


17q11 microdeletion syndrome

(no data available)