Thrombophilia, X-linked, due to factor VIII defect

Preferred Label : Thrombophilia, X-linked, due to factor VIII defect;

Symbol : THPH13;

Type : Phenotype, molecular basis known;

Prefixed ID : #301071;

Détails

Origin ID

301071;

UMLS CUI

C5676879;

Genes related to phenotype
- Coagulation factor VIII [OMIM gene]
HPO term(s)
- Adult onset [HPO term]
- Deep venous thrombosis [HPO term]
- Increased factor VIII activity [HPO term]
- Pulmonary embolism [HPO term]
- X-linked dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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