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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Marfan syndrome type 2
Idiopathic hypereosinophilic syndrome

TGFBR2 FIP1L1
PDGFRA
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TGFBR2
(0.63)
PDGFRA



Citations in the biomedical literature:


Marfan syndrome type 2
TGFBR2
Idiopathic hypereosinophilic syndrome
FIP1L1 PDGFRA PDGFRB



Marfan syndrome type 2
Idiopathic hypereosinophilic syndrome

Synonym(s):
- Loeys-Dietz syndrome type 2
- MFS2

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare surgical thoracic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.