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Descriptor English: Hyper-IgM Immunodeficiency Syndrome
Descriptor Spanish: Síndrome de Inmunodeficiencia con Hiper-IgM
Descriptor Portuguese: Síndrome de Imunodeficiência com Hiper-IgM
Descriptor French: Syndrome d'hyper-IgM
Entry term(s): HIGM2 Syndrome
HIGM2 Syndromes
HIGM3 Syndrome
HIGM3 Syndromes
HIGM5 Syndrome
HIGM5 Syndromes
Hyper IgM Immunodeficiency Syndrome
Hyper IgM Immunodeficiency Syndrome Type 2
Hyper IgM Immunodeficiency Syndrome Type 3
Hyper IgM Immunodeficiency Syndrome Type 5
Hyper IgM Immunodeficiency Syndrome, Type 2
Hyper IgM Immunodeficiency Syndrome, Type 3
Hyper IgM Immunodeficiency Syndrome, Type 5
Hyper IgM Syndrome
Hyper IgM Syndrome 2
Hyper IgM Syndrome 3
Hyper IgM Syndrome 5
Hyper-IgM Immunodeficiency Syndrome Type 2
Hyper-IgM Immunodeficiency Syndrome Type 3
Hyper-IgM Immunodeficiency Syndrome Type 5
Hyper-IgM Immunodeficiency Syndrome, Type 2
Hyper-IgM Immunodeficiency Syndrome, Type 3
Hyper-IgM Immunodeficiency Syndrome, Type 5
Hyper-IgM Immunodeficiency Syndromes
Hyper-IgM Syndrome
Hyper-IgM Syndrome 2
Hyper-IgM Syndrome 3
Hyper-IgM Syndrome 5
Hyper-IgM Syndrome 5s
Hyper-IgM Syndromes
Immunodeficiency Syndrome, Hyper-IgM
Immunodeficiency Syndromes, Hyper-IgM
Immunodeficiency with Hyper IgM Syndrome
Immunodeficiency with Hyper IgM, Type 2
Immunodeficiency with Hyper IgM, Type 3
Immunodeficiency with Hyper IgM, Type 5
Immunodeficiency with Hyper-IgM Syndrome
Immunodeficiency with Hyper-IgM, Type 2
Immunodeficiency with Hyper-IgM, Type 3
Immunodeficiency with Hyper-IgM, Type 5
Syndrome, Hyper-IgM Immunodeficiency
Syndromes, Hyper-IgM Immunodeficiency
Tree number(s): C15.378.147.333.249
C16.320.413
C16.320.798.625
C20.673.430.250
C20.673.795.625
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D053306
Scope note: A rare inherited immunodeficiency syndrome characterized by normal or elevated serum IMMUNOGLOBULIN M levels with absence of IMMUNOGLOBULIN G; IMMUNOGLOBULIN A; and IMMUNOGLOBULIN E. It results in a profound susceptibility to BACTERIAL INFECTIONS and an increased susceptibility to OPPORTUNISTIC INFECTIONS. Several subtypes of hyper-IgM immunodeficiency syndrome exist depending upon the location of genetic mutation.
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: Immunoglobulin A (1995-2006)
Immunoglobulin E (1995-2006)
Immunoglobulin G (1995-2006)
Immunoglobulin M (1995-2006)
Immunologic Deficiency Syndromes (1995-2006)
Public MeSH Note: 2007
History Note: 2007
DeCS ID: 52137
Unique ID: D053306
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2013/07/08
Hyper-IgM Immunodeficiency Syndrome - Preferred
Concept UI M0492421
Scope note A rare inherited immunodeficiency syndrome characterized by normal or elevated serum IMMUNOGLOBULIN M levels with absence of IMMUNOGLOBULIN G; IMMUNOGLOBULIN A; and IMMUNOGLOBULIN E. It results in a profound susceptibility to BACTERIAL INFECTIONS and an increased susceptibility to OPPORTUNISTIC INFECTIONS. Several subtypes of hyper-IgM immunodeficiency syndrome exist depending upon the location of genetic mutation.
Preferred term Hyper-IgM Immunodeficiency Syndrome
Entry term(s) Hyper IgM Immunodeficiency Syndrome
Hyper IgM Syndrome
Hyper-IgM Immunodeficiency Syndromes
Hyper-IgM Syndrome
Hyper-IgM Syndromes
Immunodeficiency Syndrome, Hyper-IgM
Immunodeficiency Syndromes, Hyper-IgM
Immunodeficiency with Hyper IgM Syndrome
Immunodeficiency with Hyper-IgM Syndrome
Syndrome, Hyper-IgM Immunodeficiency
Syndromes, Hyper-IgM Immunodeficiency
Hyper-IgM Immunodeficiency Syndrome, Type 5 - Narrower
Concept UI M0492428
Preferred term Hyper-IgM Immunodeficiency Syndrome, Type 5
Entry term(s) HIGM5 Syndrome
HIGM5 Syndromes
Hyper IgM Immunodeficiency Syndrome Type 5
Hyper IgM Immunodeficiency Syndrome, Type 5
Hyper IgM Syndrome 5
Hyper-IgM Immunodeficiency Syndrome Type 5
Hyper-IgM Syndrome 5
Hyper-IgM Syndrome 5s
Immunodeficiency with Hyper IgM, Type 5
Immunodeficiency with Hyper-IgM, Type 5
Hyper-IgM Immunodeficiency Syndrome, Type 2 - Narrower
Concept UI M0492422
Scope note Hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding activation-induced CYTIDINE DEAMINASE.
Preferred term Hyper-IgM Immunodeficiency Syndrome, Type 2
Entry term(s) HIGM2 Syndrome
HIGM2 Syndromes
Hyper IgM Immunodeficiency Syndrome Type 2
Hyper IgM Immunodeficiency Syndrome, Type 2
Hyper IgM Syndrome 2
Hyper-IgM Immunodeficiency Syndrome Type 2
Hyper-IgM Syndrome 2
Immunodeficiency with Hyper IgM, Type 2
Immunodeficiency with Hyper-IgM, Type 2
Hyper-IgM Immunodeficiency Syndrome, Type 3 - Narrower
Concept UI M0492427
Scope note Hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 ANTIGEN.
Preferred term Hyper-IgM Immunodeficiency Syndrome, Type 3
Entry term(s) HIGM3 Syndrome
HIGM3 Syndromes
Hyper IgM Immunodeficiency Syndrome Type 3
Hyper IgM Immunodeficiency Syndrome, Type 3
Hyper IgM Syndrome 3
Hyper-IgM Immunodeficiency Syndrome Type 3
Hyper-IgM Syndrome 3
Immunodeficiency with Hyper IgM, Type 3
Immunodeficiency with Hyper-IgM, Type 3



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