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|
Corneodermatosseous syndrome is an autosom … Corneodermatosseous syndrome is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.tature, and medullary narrowing of digits.
|
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H18.5
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C536444
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122440
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3194
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21522614
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1963
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|
893158343
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http://dbpedia.org/resource/Keratoderma +
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|
| http://dbpedia.org/property/caption
|
This condition is inherited in an autosomal dominant manner
|
| http://dbpedia.org/property/icd
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H18.5
|
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536444.0
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Corneodermatoosseous syndrom
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122440
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3194
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| http://dbpedia.org/property/synonyms
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CDO syndrome
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http://dbpedia.org/resource/Category:Syndromes_with_short_stature +
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http://dbpedia.org/resource/Condition +
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Corneodermatoosseous syndrom
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|
| rdfs:comment |
Corneodermatosseous syndrome is an autosom … Corneodermatosseous syndrome is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.tature, and medullary narrowing of digits.
|
| rdfs:label |
Corneodermatoosseous syndrome
|
