Platelet signal processing defect

Preferred Label : Platelet signal processing defect;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 173590;

Details

Origin ID

173590;

UMLS CUI

C1868199;

Currated CISMeF NLP mapping
- platelet signal processing defect [MeSH concept]
- platelet signal processing defect [MeSH Supplementary Concept]
HPO term(s)
- Abnormal bleeding [HPO term]
- Autosomal dominant inheritance [HPO term]
- Epistaxis [HPO term]
- Impaired ADP-induced platelet aggregation [HPO term]
- Impaired collagen-induced platelet aggregation [HPO term]
- Impaired epinephrine-induced platelet aggregation [HPO term]
- Thrombocytopenia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- platelet signal processing defect [MeSH Supplementary Concept]
- platelet signal processing defect [MeSH concept]

Keyword's position in hierarchy(ies) :

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