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Descriptor English: Primary Immunodeficiency Diseases
Descriptor Spanish: Enfermedades de Inmunodeficiencia Primaria
Descriptor enfermedades de inmunodeficiencia primaria
Entry term(s) deficiencia inmunitaria primaria
deficiencias primarias de anticuerpos
enfermedad por deficiencia inmunitaria primaria
enfermedad por inmunodeficiencia congénita
enfermedad por inmunodeficiencia hereditaria
enfermedad por inmunodeficiencia primaria
enfermedades de inmunodeficiencia congénita
enfermedades de inmunodeficiencia hereditaria
síndrome de deficiencia primaria de anticuerpos
síndrome de inmunodeficiencia congénita
síndrome de inmunodeficiencia hereditaria
síndrome de inmunodeficiencia primaria
síndromes de deficiencia inmunitaria primaria
síndromes de deficiencia primaria de anticuerpos
síndromes de inmunodeficiencia hereditaria
síndromes de inmunodeficiencia primaria
trastorno por deficiencia inmunitaria primaria
trastorno por deficiencia primaria de anticuerpos
trastorno por inmunodeficiencia congénita
trastorno por inmunodeficiencia hereditario
trastorno por inmunodeficiencia primaria
trastornos de deficiencia inmunitaria primaria
trastornos de deficiencia primaria de anticuerpos
trastornos de inmunodeficiencia hereditaria
trastornos de inmunodeficiencia primaria
Scope note: Enfermedades y síndromes de deficiencia inmunológica genética debida a mutaciones en genes relacionados con la INMUNIDAD que se caracterizan generalmente por un aumento de la susceptibilidad a las enfermedades infecciosas. A menudo se asocian a manifestaciones de ENFERMEDADES AUTOINMUNITARIAS.
Descriptor Portuguese: Doenças da Imunodeficiência Primária
Descriptor French: Maladies d'immunodéficience primaire
Entry term(s): Antibody Deficiency, Primary
Congenital Immunodeficiency Disease
Congenital Immunodeficiency Diseases
Congenital Immunodeficiency Disorder
Congenital Immunodeficiency Disorders
Congenital Immunodeficiency Syndrome
Congenital Immunodeficiency Syndromes
Deficiency, Primary Immune
Immune Deficiency, Primary
Immunodeficiency Disease, Congenital
Immunodeficiency Disease, Inherited
Immunodeficiency Disease, Primary
Immunodeficiency Diseases, Congenital
Immunodeficiency Diseases, Inherited
Immunodeficiency Diseases, Primary
Immunodeficiency Disorder, Congenital
Immunodeficiency Disorder, Inherited
Immunodeficiency Disorder, Primary
Immunodeficiency Disorders, Congenital
Immunodeficiency Disorders, Inherited
Immunodeficiency Syndrome, Congenital
Immunodeficiency Syndrome, Inherited
Immunodeficiency Syndrome, Primary
Immunodeficiency Syndromes, Congenital
Immunodeficiency Syndromes, Inherited
Immunodeficiency Syndromes, Primary
Inherited Immunodeficiency Disease
Inherited Immunodeficiency Diseases
Inherited Immunodeficiency Disorder
Inherited Immunodeficiency Disorders
Inherited Immunodeficiency Syndrome
Inherited Immunodeficiency Syndromes
Primary Antibody Deficiencies
Primary Antibody Deficiency
Primary Antibody Deficiency Disorder
Primary Antibody Deficiency Disorders
Primary Antibody Deficiency Syndrome
Primary Antibody Deficiency Syndromes
Primary Immune Deficiencies
Primary Immune Deficiency
Primary Immune Deficiency Disease
Primary Immune Deficiency Diseases
Primary Immune Deficiency Disorder
Primary Immune Deficiency Disorders
Primary Immune Deficiency Syndrome
Primary Immune Deficiency Syndromes
Primary Immunodeficiency Disease
Primary Immunodeficiency Disorder
Primary Immunodeficiency Disorders
Primary Immunodeficiency Syndrome
Primary Immunodeficiency Syndromes
Tree number(s): C16.320.798
C20.673.795
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000081207
Scope note: Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Immunologic Deficiency Syndromes (1972-2019)
Public MeSH Note: 2020
History Note: 2020
DeCS ID: 59201
Unique ID: D000081207
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2020/01/01
Date of Entry: 2019/07/08
Revision Date: 2020/05/27
Primary Immunodeficiency Diseases - Preferred
Concept UI M000650094
Scope note Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations.
Preferred term Primary Immunodeficiency Diseases
Entry term(s) Deficiency, Primary Immune
Immune Deficiency, Primary
Immunodeficiency Disease, Primary
Immunodeficiency Diseases, Primary
Immunodeficiency Disorder, Primary
Immunodeficiency Syndrome, Primary
Immunodeficiency Syndromes, Primary
Primary Immune Deficiencies
Primary Immune Deficiency
Primary Immune Deficiency Disease
Primary Immune Deficiency Diseases
Primary Immune Deficiency Disorder
Primary Immune Deficiency Disorders
Primary Immune Deficiency Syndrome
Primary Immune Deficiency Syndromes
Primary Immunodeficiency Disease
Primary Immunodeficiency Disorder
Primary Immunodeficiency Disorders
Primary Immunodeficiency Syndrome
Primary Immunodeficiency Syndromes
Congenital Immunodeficiency Diseases - Narrower
Concept UI M000650099
Preferred term Congenital Immunodeficiency Diseases
Entry term(s) Congenital Immunodeficiency Disease
Congenital Immunodeficiency Disorder
Congenital Immunodeficiency Disorders
Congenital Immunodeficiency Syndrome
Congenital Immunodeficiency Syndromes
Immunodeficiency Disease, Congenital
Immunodeficiency Diseases, Congenital
Immunodeficiency Disorder, Congenital
Immunodeficiency Disorders, Congenital
Immunodeficiency Syndrome, Congenital
Immunodeficiency Syndromes, Congenital
Primary Antibody Deficiencies - Narrower
Concept UI M000650103
Preferred term Primary Antibody Deficiencies
Entry term(s) Antibody Deficiency, Primary
Primary Antibody Deficiency
Primary Antibody Deficiency Disorder
Primary Antibody Deficiency Disorders
Primary Antibody Deficiency Syndrome
Primary Antibody Deficiency Syndromes
Inherited Immunodeficiency Diseases - Narrower
Concept UI M000650100
Preferred term Inherited Immunodeficiency Diseases
Entry term(s) Immunodeficiency Disease, Inherited
Immunodeficiency Diseases, Inherited
Immunodeficiency Disorder, Inherited
Immunodeficiency Disorders, Inherited
Immunodeficiency Syndrome, Inherited
Immunodeficiency Syndromes, Inherited
Inherited Immunodeficiency Disease
Inherited Immunodeficiency Disorder
Inherited Immunodeficiency Disorders
Inherited Immunodeficiency Syndrome
Inherited Immunodeficiency Syndromes



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