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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pilomatrixoma
Marfan syndrome type 2

CTNNB1 TGFBR2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.73)
TGFBR2



Citations in the biomedical literature:


Pilomatrixoma
CTNNB1
Marfan syndrome type 2
TGFBR2



Pilomatrixoma
Marfan syndrome type 2

Synonym(s):
- Epithelioma calcificans of Malherbe
- Pilomatricoma

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

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

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

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

External references:
1 OMIM reference -
1 MeSH reference: D018296
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.