Preferred Name |
Scott Syndrome |
|
Synonyms |
Prothrombin Consumption Inhibitor, Familial |
|
ID |
http://purl.bioontology.org/ontology/MESH/C563120 |
|
altLabel |
Prothrombin Consumption Inhibitor, Familial Bleeding Abnormality due to Deficiency of Platelet Binding of Factor X Prothrombin Consumption Deficiency Prothrombin Conversion Defect, Familial |
|
cui |
C0796149 |
|
HM |
D001778 |
|
Inverse of RB |
0 |
|
Mapped to | ||
MDA |
20121105 |
|
MeSH Frequency |
19 |
|
notation |
C563120 |
|
prefLabel |
Scott Syndrome |
|
SC |
3 |
|
TERMUI |
T802224 T802227 T802223 T825864 T802225 |
|
TH |
OMIM (2013) |
|
tui |
T047 |
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