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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Sporadic secreting paraganglioma
Neurofibromatosis type 3

EPAS1 LZTR1
NF2
SMARCB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EPAS1
(0.63)
SMARCB1



Citations in the biomedical literature:


Sporadic secreting paraganglioma
EPAS1
Neurofibromatosis type 3
LZTR1 NF2 SMARCB1



Sporadic secreting paraganglioma
Neurofibromatosis type 3

Synonym(s):
(no synonyms)

Synonym(s):
- NF3
- Neurilemmomatosis
- Schwannomatosis

Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare skin 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:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: C536641

No signs/symptoms info available.