Hereditary Complement Deficiency Diseases

Preferred Label : Hereditary Complement Deficiency Diseases;

MeSH definition : Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).;

MeSH synonym : Inherited Complement Deficiency Diseases;

MeSH Hyperonym : Complement Deficiency;

Wikipedia link : https://en.wikipedia.org/wiki/Complement deficiency;

Details

Origin ID

D000081208;

UMLS CUI

C5197806;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Complement deficiency [PASCAL descriptor]
DO Cross reference
- complement deficiency [DO Concept]
Record concept(s)
- Complement Deficiencies [MeSH concept]
- Hereditary Complement Deficiency Diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- C6 deficiency, subtotal [MeSH Supplementary Concept]
- C9 deficiency [MeSH Supplementary Concept]
- C9 deficiency with dermatomyositis [MeSH Supplementary Concept]
- MASP2 deficiency [MeSH Supplementary Concept]
- complement component 3 deficiency, autosomal recessive [MeSH Supplementary Concept]
- complement component 4, partial deficiency of [MeSH Supplementary Concept]
- complement component 4a deficiency [MeSH Supplementary Concept]
- complement component 5 deficiency [MeSH Supplementary Concept]
- complement component 6 deficiency [MeSH Supplementary Concept]
- complement component 7 deficiency [MeSH Supplementary Concept]
- complement component C1s deficiency [MeSH Supplementary Concept]
- complement factor D deficiency [MeSH Supplementary Concept]
- complement factor H deficiency [MeSH Supplementary Concept]
- complement factor I deficiency [MeSH Supplementary Concept]
- properdin deficiency, X-linked [MeSH Supplementary Concept]
- properdin deficiency, type II [MeSH Supplementary Concept]
- properdin deficiency, type III [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- Complement Deficiency [NCIt concept]
- Complement deficiency [HPO term]
- complement deficiency [DO Concept]

Keyword's position in hierarchy(ies) :

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