Human Disease and Mouse Model Detail
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Human Disease
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Scott Syndrome; SCTS
OMIM ID: 262890
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Synonyms
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Bleeding Abnormality Due to Deficiency of Platelet Binding of Factor X;
Bleeding Disorder, Platelet-Type, 7; BDPLT7;
Prothrombin Consumption Deficiency;
Prothrombin Consumption Inhibitor, Familial;
Prothrombin Conversion Defect, Familial
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Ano6
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ANO6*
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1:1 Homology
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Analysis Tools