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Q35923500-2A91F74B-E97E-4FE0-8643-44B1E1BBBE11
Q35923500-2A91F74B-E97E-4FE0-8643-44B1E1BBBE11
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Statement
http://www.wikidata.org/entity/statement/Q35923500-2A91F74B-E97E-4FE0-8643-44B1E1BBBE11
Keratins and skin disorders.
P2860
Q35923500-2A91F74B-E97E-4FE0-8643-44B1E1BBBE11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35923500-2A91F74B-E97E-4FE0-8643-44B1E1BBBE11
rank
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wasDerivedFrom
f0b1a59a86ca47bb66c3cdf791b9e3f4c356f9a9
P2860
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex.