Begreppsinformation
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Epidermolysis Bullosa
Föredragen term
Epidermolysis Bullosa, Junctional
Typ
-
Topical Descriptor
Överordnat begrepp
Hänvisningstermer
- Epidermolysis Bullosa, Generalized Atrophic Benign
- Epidermolysis Bullosa Junctionalis, Disentis Type
- Epidermolysis Bullosa Junctionalis, Severe Nonlethal
- Junctional Epidermolysis Bullosa
Användningsanmärkning
- Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.
Anmärkning om ändringshistoria
- 91; HERLITZ DISEASE was HERLITZ'S DISEASE 1991-92
Termer på andra språk
-
finska
-
epidermolysis bullosa junctionalis
-
epidermolysis bullosa letalis
-
Herlitz
-
Herlitzin oireyhtymä
-
Herlitzin syndrooma
-
junktionaalinen epidermolysis bullosa
-
kuolemaan johtava epidermolysis bullosa
-
syndroma Herlitz
-
svenska
URI
http://www.yso.fi/onto/mesh/D016109
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}