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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
2 associated genes
1 sign/symptom
Alveolar rhabdomyosarcoma
Familial hypospadias

FOXO1 AR
PAX3 MAMLD1
PAX7


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FOXO1
(0.9)
AR



Citations in the biomedical literature:


Alveolar rhabdomyosarcoma
FOXO1 PAX3 PAX7
Familial hypospadias
AR MAMLD1



Alveolar rhabdomyosarcoma
Familial hypospadias

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

Classification (ICD10):
- Neoplasms -
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:
1 OMIM reference -
1 MeSH reference: D018232
External references:
4 OMIM references -
No MeSH references

Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Alveolar rhabdomyosarcoma

(no data available)