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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
2 associated genes
1 sign/symptom
Peripheral primitive neuroectodermal tumor
Familial hypospadias

ERG AR
FLI1 MAMLD1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ERG
(0.75)
AR



Citations in the biomedical literature:


Peripheral primitive neuroectodermal tumor
ERG FLI1
Familial hypospadias
AR MAMLD1



Peripheral primitive neuroectodermal tumor
Familial hypospadias

Synonym(s):
- PPNET
- Peripheral PNET

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare bone disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references

Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Peripheral primitive neuroectodermal tumor

(no data available)