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Sporadic pheochromocytoma
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
4 associated genes
No signs/symptoms info
Sporadic pheochromocytoma
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

EPAS1
(UniProt - OMIM)
 MAGEL2
(UniProt - OMIM)
NDN
(UniProt - OMIM)
OCA2
(UniProt - OMIM)
SNRPN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EPAS1
(0.68)
NDN


Citations in the biomedical literature:


Sporadic pheochromocytoma
EPAS1
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
MAGEL2 NDN OCA2 SNRPN



Sporadic pheochromocytoma
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

Synonym(s):
(no synonyms)

Synonym(s):
- UPD(15)mat
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare infertility
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.