MeSH Browser

MeSH Supplementary: Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
Unique ID: C566600
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566600
Entry Term(s): KLICK Syndrome
Registry Numbers: 0
Heading Mapped to: *Skin Abnormalities; *Skin Diseases, Genetic
Frequency: 3
Note: mutation in POMP
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma MeSH Supplementary Concept Data 2025