Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
Disease Name
Lung Diseases, Obstructive
Standard Disease Name
lung diseases, obstructive
MeSH Tree
No data
ICD-10
D68.0|D69.8
Identifiers
DO ID
No data
MeSH ID
D014842
OMIM ID
MTHU016680
UMLS ID
C0042974
HPO ID
No data
Description and Extensions
Description
SNOMEDCT_US_2016_09_01:Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome|NCI2016_02D:Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding.|MSH2017_2016_08_12:Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.|CSP2006:hemophilioid disorder due to deficiency of Von Willebrand factor and thus of Factor VIII complex.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.