epidermolysis bullosa simplex of Ogna
Human disease
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epidermolysis bullosa simplex of Ogna
Summary
epidermolysis bullosa simplex of Ogna is a rare disease[1].
Key Facts
- epidermolysis bullosa simplex of Ogna's instance of is recorded as rare disease[2].
- epidermolysis bullosa simplex of Ogna's instance of is recorded as class of disease[3].
- epidermolysis bullosa simplex of Ogna is a type of epidermolysis bullosa simplex[4].
- epidermolysis bullosa simplex of Ogna is a type of basal epidermolysis bullosa simplex[5].
- epidermolysis bullosa simplex of Ogna is a type of genetic disease[6].
- epidermolysis bullosa simplex of Ogna is a type of autosomal dominant disease[7].
- epidermolysis bullosa simplex of Ogna's ICD-9-CM is recorded as 757.39[8].
- epidermolysis bullosa simplex of Ogna's health specialty is recorded as medical genetics[9].
- epidermolysis bullosa simplex of Ogna's genetic association is recorded as PLEC[10].
- epidermolysis bullosa simplex of Ogna's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060736[11].
- epidermolysis bullosa simplex of Ogna's exact match is recorded as http://identifiers.org/doid/DOID:0060736[12].
- epidermolysis bullosa simplex of Ogna's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79401[13].
- epidermolysis bullosa simplex of Ogna's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].