MeSH Browser

MeSH Supplementary: Vohwinkel Syndrome, Variant Form
Unique ID: C565826
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565826
Entry Term(s): Mutilating Keratoderma with Ichthyosis; Vohwinkel Syndrome with Ichthyosis
Registry Numbers: 0
Heading Mapped to: *Skin Diseases, Genetic
Frequency: 9
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Vohwinkel Syndrome, Variant Form MeSH Supplementary Concept Data 2024