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
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
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.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
02
(−)-Alloaromadendrene
No data
03
()-Alpha-Terpineol
No data
04
()-Borneol
No data
05
()-Cuparene
No data
06
07
08
()-Menthol
No data