junctional epidermolysis bullosa Herlitz type

Summary
Synonym
  • Herlitz type epidermolysis bullosa junctionalis
  • Herlitz-Pearson-type epidermolysis bullosa
  • JEB-H
  • JEB-Herlitz type
  • epidermolysis bullosa letalis
  • junctional epidermolysis bullosa generalisata gravis
  • junctional epidermolysis bullosa, Herlitz-Pearson type
Definition
A junctional epidermolysis bullosa characterized by autosomal recessive inheritance of severe blisters and extensive erosions, localized to the skin and mucous membranes, resulting in a failure to thrive and that has_material_basis_in mutations in any 1 of the 3 genes encoding the subunits of laminin-5: LAMA3, LAMB3, and LAMC2. The Herlitz type is more severe than the related non-Herlitz type of junctional epidermolysis bullosa.
Super Class
autosomal recessive disease junctional epidermolysis bullosa
Disease Ontology
DOID:0060737
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
3655 ITGA6 integrin subunit alpha 6
3914 LAMB3 laminin subunit beta 3
3918 LAMC2 laminin subunit gamma 2
Displaying all 3 entries
Gene ID Gene Symbol Description Source
16403 Itga6 integrin alpha 6
16780 Lamb3 laminin, beta 3
16782 Lamc2 laminin, gamma 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
32275 mew multiple edematous wings
Displaying 1 entry
Gene ID Gene Symbol Description Source
176296 ina-1 Integrin alpha ina-1

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024