ODCs

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5 OMIM references -
4 associated genes
11 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Nephroblastoma

Cerebellar ataxia-deafness-narcolepsy syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	WT1	(0.63)	DNMT1

Citations in the biomedical literature:

Nephroblastoma		Cerebellar ataxia-deafness-narcolepsy syndrome
	Synonym(s): - Renal embryonic tumor - Wilms tumor		Synonym(s): - ADCA-DN - Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome

	Classification (Orphanet): - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): (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		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	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
Cerebellar ataxia-deafness-narcolepsy syndrome
(no data available)