Acrokeratoderma, hereditary papulotranslucent

Preferred Label : Acrokeratoderma, hereditary papulotranslucent;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 101840;

Details

Origin ID

101840;

UMLS CUI

C1863343;

Currated CISMeF NLP mapping
- acrokeratoderma, hereditary papulotranslucent [MeSH concept]
- acrokeratoderma, hereditary papulotranslucent [MeSH Supplementary Concept]
- hereditary papulotranslucent acrokeratoderma [DO Concept]
DO Cross reference
- hereditary papulotranslucent acrokeratoderma [DO Concept]
HPO term(s)
- Allergy [HPO term]
- Autosomal dominant inheritance [HPO term]
- Fine hair [HPO term]
- Papule [HPO term]
- Skin plaque [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- acrokeratoderma, hereditary papulotranslucent [MeSH Supplementary Concept]
- acrokeratoderma, hereditary papulotranslucent [MeSH concept]
- hereditary papulotranslucent acrokeratoderma [DO Concept]

Keyword's position in hierarchy(ies) :

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