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1 OMIM reference -
1 associated gene
7 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Denys-Drash syndrome
Limb-mammary syndrome

WT1 TP63


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WT1
(0.55)
TP63



Citations in the biomedical literature:


Denys-Drash syndrome
WT1
Limb-mammary syndrome
TP63



Denys-Drash syndrome
Limb-mammary syndrome

Synonym(s):
- Drash syndrome
- Wilms tumor and pseudohermaphroditism

Synonym(s):
- LMS

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease
- Rare renal disease
- Rare urogenital disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare skin disease

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D030321
External references:
1 OMIM reference -
1 MeSH reference: C535903

Denys-Drash syndrome

Very frequent
- Male pseudohermaphrodism / lack of virilisation
- Nephroblastoma / Wilms tumor
- Nephrotic syndrome
- Proteinuria
- Renal disease / nephropathy

Frequent
- Chronic arterial hypertension

Occasional
- Mixed gonadal dysgenesis


Limb-mammary syndrome

(no data available)