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4 OMIM references -
2 associated genes
1 sign/symptom
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Familial hypospadias
Generalized juvenile polyposis/juvenile polyposis coli

AR BMPR1A
MAMLD1 ENG
SMAD4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AR
(0.88)
SMAD4



Citations in the biomedical literature:


Familial hypospadias
AR MAMLD1
Generalized juvenile polyposis/juvenile polyposis coli
BMPR1A ENG SMAD4



Familial hypospadias
Generalized juvenile polyposis/juvenile polyposis coli

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

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

Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Generalized juvenile polyposis/juvenile polyposis coli

(no data available)