Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
(min 2 characters)

Netherton Syndrome

"Netherton Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

Expand or collapse the group MeSH information
Rare autosomal recessive disease with variable expressions. Clinical features of the disease include variable ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; bamboo hair (trichorrhexis invaginata); and ATOPIC DERMATITIS. The disease is caused by mutations in the SPINK5 gene.


Expand or collapse the group publications
This graph shows the total number of publications written about "Netherton Syndrome" by people in this website by year, and whether "Netherton Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.