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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
29 OMIM references -
16 associated genes
No signs/symptoms info
Sporadic pheochromocytoma
Autosomal recessive nonsyndromic intellectual deficit

EPAS1 CC2D1A
CRADD
CRBN
GRIK2
KIAA1033
LINS
MAN1B1
MED13L
MED23
NSUN2
PRSS12
ST3GAL3
TECR
TRAPPC9
TUSC3
ZC3H14


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EPAS1
(0.63)
MED23



Citations in the biomedical literature:


Sporadic pheochromocytoma
EPAS1
Autosomal recessive nonsyndromic intellectual deficit
CC2D1A CRADD CRBN GRIK2 KIAA1033 LINS
MAN1B1 MED13L MED23 NSUN2 PRSS12 ST3GAL3
TECR TRAPPC9 TUSC3 ZC3H14



Sporadic pheochromocytoma
Autosomal recessive nonsyndromic intellectual deficit

Synonym(s):
(no synonyms)

Synonym(s):
- NS-ARID

Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
29 OMIM references -
No MeSH references

No signs/symptoms info available.