01
Diseases
Severe Hereditary Thrombophilia Due To Congenital Protein C Deficiency
severe hereditary thrombophilia due to congenital protein c deficiency
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.
Core Information
- Disease Name
- Severe Hereditary Thrombophilia Due To Congenital Protein C Deficiency
- Standard Disease Name
- severe hereditary thrombophilia due to congenital protein c deficiency
- MeSH Tree
- No data
- ICD-10
- D68.2
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 612304|176860
- UMLS ID
- C2930896|C0398625
- HPO ID
- No data
Description and Extensions
- Description
- Congenital protein C deficiency is an inherited coagulation disorder characterized by deep venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein C.