MeSH Browser

MeSH Supplementary: Ichthyosiform erythroderma, corneal involvement, deafness
Unique ID: C537363
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537363
Entry Term(s): Desmons syndrome; Ichthyosiform Erythroderma, Corneal Involvement, And Deafness; Keratitis-ichthyosis-deafness syndrome, autosomal recessive; Kid Syndrome, Autosomal Recessive
Registry Number: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary; *Deafness; *Ichthyosis, Lamellar
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Ichthyosiform erythroderma, corneal involvement, deafness MeSH Supplementary Concept Data 2024