Cytoscape Web
Click node...

Familial retinoblastoma
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial hypospadias
4 OMIM references -
2 associated genes
1 sign/symptom
Familial retinoblastoma
Familial hypospadias

RB1
(UniProt - OMIM)
 AR
(UniProt - OMIM)
MAMLD1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RB1
(0.89)
AR


Citations in the biomedical literature:


Familial retinoblastoma
RB1
Familial hypospadias
AR MAMLD1



Familial retinoblastoma
Familial hypospadias

Synonym(s):
- Bilateral retinoblastoma
- Hereditary retinoblastoma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- 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:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
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



Familial retinoblastoma

(no data available)