Disease #01774 (epidermolysis bullosa, junctional, non-Herlitz type, OMIM:226650)

Official abbreviation -
Name epidermolysis bullosa, junctional, non-Herlitz type
OMIM ID 226650
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 5 genes COL17A1, ITGB4, LAMA3, LAMB3, LAMC2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00306211 111 - - F - China - - - - - epidermolysis bullosa, junctional, non-Herlitz type - COL17A1 COL17A1 2 1 Sha Hong
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