Defects in the complement system

Preferred Label : Defects in the complement system;

Inclusion CIM-10 : C1 esterase inhibitor [C1-INH] deficiency;

Diag associé à un acte (%) : 54.6;

Source : OMS;

Date de début : 01/01/1997;

Détails

Origin ID

D841;

UMLS CUI

C0272242;

Automatic exact mappings (from CISMeF team)
- Anomalies of complement [HRDO Sign]
Currated CISMeF NLP mapping
- Complement Deficiency [NCIt concept]
- Complement deficiency [PASCAL descriptor]
- Complement deficiency [HPO term]
- Complement deficiency disease [MedDRA Preferred Term]
- Complement deficiency disease (disorder) [SNOMED CT concept]
- Defects in the complement system [ICD-11 Subcategory]
- complement deficiency [Disease (Nov.)]
- complement deficiency [DO Concept]
- complement deficiency disease, nos [SNOMED Notion]
DO Cross reference
- complement component 2 deficiency [DO Concept]
- complement component 4a deficiency [DO Concept]
- complement component 4b deficiency [DO Concept]
- complement component 6 deficiency [DO Concept]
- complement component 7 deficiency [DO Concept]
- complement component 9 deficiency [DO Concept]
- complement deficiency [DO Concept]
- type I complement component 8 deficiency [DO Concept]
- type II complement component 8 deficiency [DO Concept]
Orphanet concepts
- ANGPT1-related hereditary angioedema with normal C1Inh [ORDO Disease]
- Acquired angioedema with C1Inh deficiency [ORDO Disease]
- C1 inhibitor deficiency [ORDO Disease]
- Complement component 3 deficiency [ORDO Disease]
- F12-related hereditary angioedema with normal C1Inh [ORDO Disease]
- Hereditary angioedema [ORDO Disease]
- Hereditary angioedema type 1 [ORDO Disease]
- Hereditary angioedema type 2 [ORDO Disease]
- Hereditary angioedema with C1Inh deficiency [ORDO Disease]
- Hereditary angioedema with normal C1Inh [ORDO Disease]
- Immunodeficiency due to MASP-2 deficiency [ORDO Disease]
- Immunodeficiency due to a classical component pathway complement deficiency [ORDO Disease]
- Immunodeficiency due to a complement cascade protein anomaly [ORDO Disease]
- Immunodeficiency due to a late component of complement deficiency [ORDO Disease]
- Immunodeficiency due to ficolin3 deficiency [ORDO Disease]
- Immunodeficiency with factor H anomaly [ORDO Disease]
- Immunodeficiency with factor I anomaly [ORDO Disease]
- PLG-related hereditary angioedema with normal C1Inh [ORDO Disease]
- Primary CD59 deficiency [ORDO Disease]
- Properdin deficiency [ORDO Disease]
- Recurrent Neisseria infections due to factor D deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Complement Deficiency [NCIt concept]
- Complement deficiency [HPO term]
- Complement deficiency [PASCAL descriptor]
- Complement deficiency disease [MedDRA Preferred Term]
- Complement deficiency disease (disorder) [SNOMED CT concept]
- Defects in the complement system [ICD-11 Subcategory]
- complement deficiency [DO Concept]
- complement deficiency [Disease (Nov.)]
- complement deficiency disease, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Hereditary angioedema type II [ICD-11 More detail]
- type I complement component 8 deficiency [DO Concept]
- type II complement component 8 deficiency [DO Concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients