Mitis junctional epidermolysis bullosa
human disease
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Summary
Mitis junctional epidermolysis bullosa is a class of disease[1].
Key Facts
- Mitis junctional epidermolysis bullosa's instance of is recorded as class of disease[2].
- Mitis junctional epidermolysis bullosa is a type of junctional epidermolysis bullosa[3].
- Mitis junctional epidermolysis bullosa is a type of genetic disease[4].
- Mitis junctional epidermolysis bullosa is a type of autosomal recessive disease[5].
- Mitis junctional epidermolysis bullosa's genetic association is recorded as COL17A1[6].
- Mitis junctional epidermolysis bullosa's genetic association is recorded as LAMB3[7].
- Mitis junctional epidermolysis bullosa's exact match is recorded as http://identifiers.org/doid/DOID:0060738[8].
- Mitis junctional epidermolysis bullosa's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060738[9].
- Mitis junctional epidermolysis bullosa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79402[10].
- Mitis junctional epidermolysis bullosa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_89840[11].
- Mitis junctional epidermolysis bullosa's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].