| Descriptor English: | Hyper-IgM Immunodeficiency Syndrome, Type 1 | ||||||
| Descriptor Spanish: |
Síndrome de Inmunodeficiencia con Hiper-IgM Tipo 1
| ||||||
| Descriptor Portuguese: | Síndrome de Imunodeficiência com Hiper-IgM Tipo 1 | ||||||
| Descriptor French: | Syndrome d'hyper-IgM lié à l'X | ||||||
| Entry term(s): |
HIGM1 HIGM1 Syndrome HIGM1 Syndromes Hyper IgM Immunodeficiency Syndrome, Type 1 Hyper IgM Immunodeficiency, X Linked Hyper IgM Syndrome 1 Hyper-IgM Immunodeficiencies, X-Linked Hyper-IgM Immunodeficiency, X-Linked Hyper-IgM Syndrome 1 Immunodeficiencies, X-Linked Hyper-IgM Immunodeficiency with Hyper IgM, Type 1 Immunodeficiency with Hyper-IgM, Type 1 Immunodeficiency, X-Linked Hyper-IgM X Linked Hyper IgM Syndrome X-Linked Hyper IgM Syndrome X-Linked Hyper-IgM Immunodeficiencies X-Linked Hyper-IgM Immunodeficiency |
||||||
| Tree number(s): |
C15.378.147.333.249.500 C16.320.322.237 C16.320.798.625.500 C20.673.430.250.500 C20.673.795.625.500 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D053307 | ||||||
| Scope note: | An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND. |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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: |
CD40 Ligand (2000-2006) Immunologic Deficiency Syndromes (1995-2006) |
||||||
| Public MeSH Note: | 2007 |
||||||
| History Note: | 2007 |
||||||
| DeCS ID: | 52138 | ||||||
| Unique ID: | D053307 | ||||||
| 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: | 2016/06/28 |
|
|
Hyper-IgM Immunodeficiency Syndrome, Type 1
- Preferred
| Concept UI |
M0492429 |
| Scope note | An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND. |
| Preferred term | Hyper-IgM Immunodeficiency Syndrome, Type 1 |
| Entry term(s) |
HIGM1 HIGM1 Syndrome HIGM1 Syndromes Hyper IgM Immunodeficiency Syndrome, Type 1 Hyper IgM Immunodeficiency, X Linked Hyper IgM Syndrome 1 Hyper-IgM Immunodeficiencies, X-Linked Hyper-IgM Immunodeficiency, X-Linked Hyper-IgM Syndrome 1 Immunodeficiencies, X-Linked Hyper-IgM Immunodeficiency with Hyper IgM, Type 1 Immunodeficiency with Hyper-IgM, Type 1 Immunodeficiency, X-Linked Hyper-IgM X Linked Hyper IgM Syndrome X-Linked Hyper IgM Syndrome X-Linked Hyper-IgM Immunodeficiencies X-Linked Hyper-IgM Immunodeficiency |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
