Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Preferred Label : Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency;

ICD-11 synonym : Hereditary thrombophilia due to congenital HRG - [histidine-rich (poly-L) glycoprotein] deficiency; Hereditary thrombophilia due to congenital HRG deficiency;

Details

Origin ID

1764310021;

Automatic exact mappings (from CISMeF team)
- thrombophilia due to HRG deficiency [DO Concept]
Currated CISMeF NLP mapping
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency [ORDO Disease]
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder) [SNOMED CT concept]
- Thrombophilia due to histidine-rich glycoprotein deficiency [OMIM Phenotype]
- histidine rich glycoprotein deficiency [Disease (Nov.)]
- thrombophilia due to Histidine-Rich glycoprotein deficiency [MeSH concept]
- thrombophilia due to elevated Histidine-Rich glycoprotein [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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