agammaglobulinemia

Preferred Label : agammaglobulinemia;

MeSH definition : An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood.;

MeSH synonym : agammaglobulinemias;

Wikipedia automatic translation : X-linked agammaglobulinemia;

Related MeSH term : hypogammaglobulinemia; Hypogammaglobulinemias;

MeSH annotation : DYSGAMMAGLOBULINEMIA is also available;

Wikipedia link : https://en.wikipedia.org/wiki/X-linked agammaglobulinemia;

Details

Origin ID

D000361;

UMLS CUI

C0001768;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [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)
- Agammaglobulinemia, X-linked [OMIM Phenotype]
- Bruton's agammaglobulinaemia [MedDRA Preferred Term]
- Bruton's agammaglobulinemia [PASCAL descriptor]
- Bruton's agammaglobulinemia [MedDRA LLT]
- Nonfamilial hypogammaglobulinaemia [ICD-10 Sub-category (who)]
- Severe combined immunodeficiency due to DCLRE1C deficiency [ORDO Disease]
- X-Linked Agammaglobulinemia [NCIt concept]
- x-linked agammaglobulinemia [SNOMED Notion]
Currated CISMeF NLP mapping
- Agammaglobulinaemia [MedDRA LLT]
- Agammaglobulinemia [PASCAL descriptor]
- Agammaglobulinemia [OMIM phenotypic series]
- Agammaglobulinemia [HPO term]
- Agammaglobulinemia [ORDO Disease]
- Agammaglobulinemia [MedDRA LLT]
- Agammaglobulinemia (finding) [SNOMED CT concept]
- Decreased circulating antibody level [HPO term]
- Hypogammaglobulinaemia [MedDRA Preferred Term]
- Hypogammaglobulinaemia NOS [MedDRA LLT]
- Hypogammaglobulinemia [NCIt concept]
- Hypogammaglobulinemia [MedDRA LLT]
- Hypogammaglobulinemia (finding) [SNOMED CT concept]
- IMMUNOGLOBULINS DECREASED [WHO-ART Preferred Term]
- agammaglobulinemia [DO Concept]
- agammaglobulinemia [Disease (Nov.)]
- agammaglobulinemia, nos [SNOMED Notion]
- hypogammaglobulinemia [Disease (Nov.)]
DO Cross reference
- agammaglobulinemia [DO Concept]
HPO term
- Agammaglobulinemia [HPO term]
- Decreased circulating antibody level [HPO term]
Manual BTNT mappings - CISMeF
- Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome [ORDO Disease]
- Autosomal agammaglobulinemia [ORDO Disease]
- ICF syndrome [ORDO Disease]
- Immunodeficiency predominantly affecting antibody production [ORDO Disease]
- Severe combined immunodeficiency [ORDO Disease]
ORDO relation(s)
- Agammaglobulinemia [ORDO Disease]
Record concept(s)
- agammaglobulinemia [MeSH concept]
- hypogammaglobulinemia [MeSH concept]
Related MeSH Supplementary Concept(s)
- achondroplasia and swiss type agammaglobulinemia [MeSH Supplementary Concept]
- agammaglobulinemia, Non-Bruton type, autosomal dominant [MeSH Supplementary Concept]
- agammaglobulinemia, X-linked, type 2 [MeSH Supplementary Concept]
- agammaglobulinemia, microcephaly, and severe dermatitis [MeSH Supplementary Concept]
- agammaglobulinemia, non-Bruton type [MeSH Supplementary Concept]
- bruton type agammaglobulinemia [MeSH Supplementary Concept]
- frenkel russe syndrome [MeSH Supplementary Concept]
- granulocytopenia with immunoglobulin abnormality [MeSH Supplementary Concept]
- hypogammaglobulinemia and isolated growth hormone deficiency, X-linked [MeSH Supplementary Concept]
- hypogammaglobulinemia, X-Linked [MeSH Supplementary Concept]
- leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema [MeSH Supplementary Concept]
- leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia [MeSH Supplementary Concept]
- microcephaly with chemotactic defect and transient hypogammaglobulinemia [MeSH Supplementary Concept]
- osteopetrosis, autosomal recessive 7 [MeSH Supplementary Concept]
- say barber miller syndrome [MeSH Supplementary Concept]
- severe combined immunodeficiency due to adenosine deaminase deficiency [MeSH Supplementary Concept]
SNOMED CT : localisation
- immune system [MeSH Descriptor]
See also
- protein-losing enteropathies [MeSH Descriptor]
See also (suggested by CISMeF)
- dysgammaglobulinemia [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Agammaglobulinaemia [MedDRA LLT]
- Agammaglobulinemia [MedDRA LLT]
- Agammaglobulinemia [ORDO Disease]
- Agammaglobulinemia [HPO term]
- Agammaglobulinemia [PASCAL descriptor]
- Agammaglobulinemia (finding) [SNOMED CT concept]
- agammaglobulinemia [Disease (Nov.)]
- agammaglobulinemia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- X-linked agammaglobulinemia [ORDO Disease]
- X-linked agammaglobulinemia (disorder) [SNOMED CT concept]

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