Phenotype Library | Search Phenotypes

Cloves Syndrome (MONDO:0013038)

A syndromic disease characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, Epidermal nevi, and Skeletal anomaly.

Overview

Category

integumentary system disorder

syndromic disease

Ontology ID

MONDO:0013038

Internal:14076

Synonyms

CLOVE syndrome, somatic

CLOVES syndrome

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

CLOVE syndrome

congenital lipomatous overgrowth - vascular malformation - epidermal nevi

congenital lipomatous overgrowth, vascular malformations, Epidermal nevi, and skeletal/spinal abnormalities

congenital lipomatous overgrowth, vascular malformations, and EPIDERMAL nevi

Mapped terms

DOID:0080351

GARD:0010939

MEDGEN:442876

MESH:C567863

NCIT:C177122

NORD:979

OMIM:612918

Orphanet:140944

SCTID:719475006

UMLS:C2752042

Child terms

Unknown children.

Results

Cookie consent