Athrombia, essential

Preferred Label : Athrombia, essential;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 209050;

Details

Origin ID

209050;

UMLS CUI

C1859595;

Currated CISMeF NLP mapping
- athrombia, essential [MeSH concept]
- athrombia, essential [MeSH Supplementary Concept]
HPO term(s)
- Abnormal bleeding [HPO term]
- Autosomal recessive inheritance [HPO term]
- Impaired platelet adhesion [HPO term]
- Impaired platelet aggregation [HPO term]
- Prolonged bleeding time [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- athrombia, essential [MeSH Supplementary Concept]
- athrombia, essential [MeSH concept]

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