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Q38265975-1C10EF4F-2D64-4A70-9361-4356380B1857
Q38265975-1C10EF4F-2D64-4A70-9361-4356380B1857
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38265975-1C10EF4F-2D64-4A70-9361-4356380B1857
Epidermal barrier disorders and corneodesmosome defects.
P2860
Q38265975-1C10EF4F-2D64-4A70-9361-4356380B1857
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38265975-1C10EF4F-2D64-4A70-9361-4356380B1857
rank
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type
BestRank
Statement
wasDerivedFrom
0d8b06bc2299abd42d31b4f1a8ac51ca65410b1f
P2860
Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A.