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General Information
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| Term |
autosomal dominant thrombophilia due to protein C deficiency |
ID (Ontology) |
DOID:0111909 (Human Disease) |
| Definition |
A thrombophilia characterized by reduced serum levels or impaired activity of PROC and in some patients recurrent venous thrombosis that has_material_basis_in heterozygous mutation in the PROC gene on chromosome 2q14.3. |
| Also Known As |
"autosomal dominant PROC deficiency" ; "autosomal dominant protein C deficiency" ; "THPH3" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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autosomal dominant thrombophilia due to protein C deficiency | 1 | for disease ribbon | autosomal dominant thrombophilia due to protein C deficiency | 1 | model of | autosomal dominant thrombophilia due to protein C deficiency | 1 |
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Relationships