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- Q17120550 subject Q7215483.
- Q17120550 subject Q8482266.
- Q17120550 abstract "Peeling skin syndrome (also known as "Acral peeling skin syndrome," "Continual peeling skin syndrome," "Familial continual skin peeling," "Idiopathic deciduous skin," and "Keratolysis exfoliativa congenita") is an autosomal recessive disorder characterized by lifelong peeling of the stratum corneum, and may be associated with pruritus, short stature, and easily removed anagen hair.The acral form can be associated with TGM5.".
- Q17120550 icd10 "Q80.8".
- Q17120550 omim "270300".
- Q17120550 wikiPageWikiLink Q10121959.
- Q17120550 wikiPageWikiLink Q17140373.
- Q17120550 wikiPageWikiLink Q199602.
- Q17120550 wikiPageWikiLink Q2038676.
- Q17120550 wikiPageWikiLink Q246809.
- Q17120550 wikiPageWikiLink Q7215483.
- Q17120550 wikiPageWikiLink Q7670170.
- Q17120550 wikiPageWikiLink Q8482266.
- Q17120550 icd "Q80.8".
- Q17120550 name "Peeling skin syndrome".
- Q17120550 omim "270300".
- Q17120550 type Disease.
- Q17120550 type Thing.
- Q17120550 type Q12136.
- Q17120550 comment "Peeling skin syndrome (also known as "Acral peeling skin syndrome," "Continual peeling skin syndrome," "Familial continual skin peeling," "Idiopathic deciduous skin," and "Keratolysis exfoliativa congenita") is an autosomal recessive disorder characterized by lifelong peeling of the stratum corneum, and may be associated with pruritus, short stature, and easily removed anagen hair.The acral form can be associated with TGM5.".
- Q17120550 label "Peeling skin syndrome".
- Q17120550 name "Peeling skin syndrome".