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

AR
(UniProt - OMIM)
 C11ORF95
(UniProt - OMIM)
MAMLD1
(UniProt - OMIM)
 RELA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
AR
(0.65)
RELA


Citations in the biomedical literature:


Familial hypospadias
AR MAMLD1
Anaplastic ependymoma
C11ORF95 RELA



Familial hypospadias
Anaplastic ependymoma

Synonym(s):
(no synonyms)

Synonym(s):
- High-grade ependymoma
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Anaplastic ependymoma

(no data available)