epidermolysis bullosa simplex with pyloric atresia
Epidermolysis bullosa simplex with pyloric atresia (EBS-PA) is a basal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized severe blistering with widespread congenital absence of skin and pyloric atresia
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epidermolysis bullosa simplex with pyloric atresia
Summary
epidermolysis bullosa simplex with pyloric atresia is a rare disease[1].
Key Facts
- epidermolysis bullosa simplex with pyloric atresia's instance of is recorded as rare disease[2].
- epidermolysis bullosa simplex with pyloric atresia's instance of is recorded as class of disease[3].
- epidermolysis bullosa simplex with pyloric atresia's subclass of is recorded as basal epidermolysis bullosa simplex[4].
- epidermolysis bullosa simplex with pyloric atresia's subclass of is recorded as pyloric atresia[5].
- epidermolysis bullosa simplex with pyloric atresia's MeSH descriptor ID is recorded as C567408[6].
- epidermolysis bullosa simplex with pyloric atresia's OMIM ID is recorded as 612138[7].
- epidermolysis bullosa simplex with pyloric atresia's Orphanet ID is recorded as 158684[8].
- epidermolysis bullosa simplex with pyloric atresia's genetic association is recorded as PLEC[9].
- epidermolysis bullosa simplex with pyloric atresia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_158684[10].
- epidermolysis bullosa simplex with pyloric atresia's UMLS CUI is recorded as C2677349[11].
- epidermolysis bullosa simplex with pyloric atresia's ICD-10-CM is recorded as Q81.0[12].
- epidermolysis bullosa simplex with pyloric atresia's Mondo ID is recorded as MONDO_0012807[13].
- epidermolysis bullosa simplex with pyloric atresia's ICD-11 ID is recorded as 1648939146[14].