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Genodermatosis

Go to external page http://purl.obolibrary.org/obo/NCIT_C156032

A group of inherited skin disorders that present with multisystem involvement. It includes ichthyosis, epidermolysis bullosa, ectodermal dysplasia, cutis laxa, progeroid conditions, xeroderma pigmentosum, Rothmund Thomson syndrome, and dyskeratosis congenita. [ ]

Term info

Label

Genodermatosis

Synonyms
  • Genodermatosis
Subsets

NCIT_C118168, NCIT_C116977

Display Name

Genodermatosis

Preferred Name

Genodermatosis

Semantic Type

Disease or Syndrome

UMLS CUI

C0037277

code

C156032

Term relations