ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Hyper-IgM Immunodeficiency Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Protein Disorders ∟ Dysgammaglobulinemia ∟ Hyper-IgM Immunodeficiency Syndrome 2 coordinate concepts 1 subordinate concept ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 ∟ IgA Deficiency \| ∟ IgG Deficiency Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Immunologic Deficiency Syndromes ∟ Dysgammaglobulinemia ∟ Hyper-IgM Immunodeficiency Syndrome 2 coordinate concepts 1 subordinate concept ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 ∟ IgA Deficiency \| ∟ IgG Deficiency X
Broader terms:	Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Protein Disorders ∟ Dysgammaglobulinemia ∟ Hyper-IgM Immunodeficiency Syndrome Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Immunologic Deficiency Syndromes ∟ Dysgammaglobulinemia ∟ Hyper-IgM Immunodeficiency Syndrome Dysgammaglobulinemia > Blood Protein Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Dysgammaglobulinemia > Immunologic Deficiency Syndromes > Immune System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Hyper-IgM Immunodeficiency Syndrome, Type 1 X
History note:	Immunoglobulin A (1995-2006) \| Immunoglobulin E (1995-2006) \| Immunoglobulin G (1995-2006) \| Immunoglobulin M (1995-2006) \| Immunologic Deficiency Syndromes (1995-2006)X
historyNote*:	2007 X
publicMeSHNote*:	2007 X
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. X
activeMeSHYear*:	2007X
dateCreated*:	2006-07-05X
dateEstablished*:	2007-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	jmpX
Type:	Concept X
Coordinate terms:	IgA Deficiency \| IgG Deficiency X
URI:	X
Labels and equivalent concepts:	Hyper-IgM-immuunivajausoireyhtymä (fi) Hyper-IgM Syndrome 2 (en, replaced) Hyper-IgM Syndrome 3 (en, replaced) Hyper-IgM Syndrome 5 (en, replaced) Immunodeficiency with Hyper-IgM Syndrome (en, replaced) Hyper-IgM Syndrome (en, replaced) Hyper-IgM Immunodeficiency Syndrome Type 5 (en, replaced) HIGM3 Syndrome (en, replaced) HIGM5 Syndrome (en, replaced) Hyper-IgM Immunodeficiency Syndrome Type 2 (en, replaced) Hyper-IgM Immunodeficiency Syndrome Type 3 (en, replaced) HIGM2 Syndrome (en, replaced) X
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