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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
CLOVE syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

PIK3CA PIK3CA


COMMON
GENES
PIK3CA



Citations in the biomedical literature:


CLOVE syndrome
PIK3CA
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia



CLOVE syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

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

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

No signs/symptoms info available.