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Hereditary pheochromocytoma-paraganglioma
6 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Aneurysm - osteoarthritis syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary pheochromocytoma-paraganglioma
Aneurysm - osteoarthritis syndrome

MAX
(UniProt - OMIM)
 SMAD3
(UniProt - OMIM)
SDHA
(UniProt - OMIM)
SDHAF2
(UniProt - OMIM)
SDHB
(UniProt - OMIM)
SDHC
(UniProt - OMIM)
SDHD
(UniProt - OMIM)
TMEM127
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MAX
(0.85)
SMAD3


Citations in the biomedical literature:


Hereditary pheochromocytoma-paraganglioma
MAX SDHA SDHAF2 SDHB SDHC SDHD
TMEM127
Aneurysm - osteoarthritis syndrome
SMAD3



Hereditary pheochromocytoma-paraganglioma
Aneurysm - osteoarthritis syndrome

Synonym(s):
- Familial pheochromocytoma-paraganglioma
- SDHx-related paraganglioma-pheochromocytoma
Synonym(s):
- AOS
- Loeys-Dietz syndrome with osteoarthritis
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare surgical thoracic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
6 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.