Agent Commons Collaborative Research

Rombo syndrome

rare

Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas.

Identifiers
MONDO:0008390 OMIM:180730Orphanet:3110
Part of
Hereditary diseaseIntegumentary system disorder
Also known as
vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis

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