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- Schöpf–Schulz–Passarge_syndrome abstract "Schöpf–Schulz–Passarge syndrome (also known as "Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.It was characterized in 1971.It has been associated with WNT10A.".
- Schöpf–Schulz–Passarge_syndrome wikiPageID "21522840".
- Schöpf–Schulz–Passarge_syndrome wikiPageRevisionID "593010192".
- Schöpf–Schulz–Passarge_syndrome icd "Q82.8".
- Schöpf–Schulz–Passarge_syndrome name "Schöpf–Schulz–Passarge syndrome".
- Schöpf–Schulz–Passarge_syndrome omim "224750".
- Schöpf–Schulz–Passarge_syndrome subject Category:Palmoplantar_keratodermas.
- Schöpf–Schulz–Passarge_syndrome type Disease.
- Schöpf–Schulz–Passarge_syndrome type Situation.
- Schöpf–Schulz–Passarge_syndrome comment "Schöpf–Schulz–Passarge syndrome (also known as "Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.It was characterized in 1971.It has been associated with WNT10A.".
- Schöpf–Schulz–Passarge_syndrome label "Schöpf–Schulz–Passarge syndrome".
- Schöpf–Schulz–Passarge_syndrome sameAs Sch%C3%B6pf%E2%80%93Schulz%E2%80%93Passarge_syndrome.
- Schöpf–Schulz–Passarge_syndrome sameAs Q7433355.
- Schöpf–Schulz–Passarge_syndrome sameAs Q7433355.
- Schöpf–Schulz–Passarge_syndrome wasDerivedFrom Schöpf–Schulz–Passarge_syndrome?oldid=593010192.