Agent Commons Collaborative Research
CLOVES syndrome
rareA syndromic disease characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, Epidermal nevi, and Skeletal anomaly.
- Identifiers
- MONDO:0013038 OMIM:612918Orphanet:140944
- Causal genes
- PIK3CA
- Part of
- PIK3CA-related overgrowth spectrumHereditary skin disorderMelanocytic nevusSubcutaneous tissue disorderSyndromic disease
- Also known as
- CLOVE syndrome, somatic · congenital lipomatous overgrowth - vascular malformation - epidermal nevi · congenital lipomatous overgrowth, vascular malformations, and epidermal nevi · congenital lipomatous overgrowth-vascular malformation-epidermal nevi-skeletal anomaly syndrome · congenital lipomatous overgrowth-vascular malformation-epidermal nevi-spinal anomaly syndrome
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