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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
CLOVE syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1D

PIK3CA DNAJB6


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PIK3CA
(0.63)
DNAJB6



Citations in the biomedical literature:


CLOVE syndrome
PIK3CA
Autosomal dominant limb-girdle muscular dystrophy type 1D
DNAJB6



CLOVE syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1D

Synonym(s):
- Congenital lipomatous overgrowth - vascular malformation - epidermal nevi

Synonym(s):
- LGMD1D

Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.