X-linked SCID

X-linked SCID
noun
SCID in male children resulting from mutation of a gene that codes for a protein on the surface of T cells that allows them to develop a growth factor receptor
Syn: ↑X-SCID

Useful english dictionary. 2012.

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  • SCID — noun a congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of life • Syn:… …   Useful english dictionary

  • SCID-X1 — Klassifikation nach ICD 10 D81.1 Schwerer kombinierter Immundefekt [SCID] mit niedriger T und B Zellen Zahl …   Deutsch Wikipedia

  • X-SCID — noun SCID in male children resulting from mutation of a gene that codes for a protein on the surface of T cells that allows them to develop a growth factor receptor • Syn: ↑X linked SCID • Hypernyms: ↑severe combined immunodeficiency, ↑severe… …   Useful english dictionary

  • X-SCID — Klassifikation nach ICD 10 D81.1 Schwerer kombinierter Immundefekt [SCID] mit niedriger T und B Zellen Zahl …   Deutsch Wikipedia

  • X-linked agammaglobulinemia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 1728 ICD10 = ICD10|D|80|0|d|80 ICD9 = ICD9|279.04 ICDO = OMIM = 300300 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 294 eMedicine mult = eMedicine2|derm|858 | MeshID = X linked… …   Wikipedia

  • X-SCID — Infobox Disease Name = X SCID Caption = DiseasesDB = 33502 ICD10 = ICD10|D|80|0|d|80 ICD9 = ICD9|279.2 ICDO = OMIM = 300400 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D053632X linked Severe Combined Immunodeficiency (X SCID) is a… …   Wikipedia

  • Severe combined immunodeficiency — Infobox Disease Name = Severe combined immunodeficiency Caption = DiseasesDB = 11978 ICD10 = ICD10|D|81|0|d|80 ICD10|D|81|2|d|80 ICD9 = ICD9|279.2 ICDO = OMIM = MedlinePlus = eMedicineSubj = med eMedicineTopic = 2214 MeshID = D016511 Severe… …   Wikipedia

  • IL2RG — (interleukin 2 receptor, gamma (severe combined immunodeficiency)) is a human gene that provides instructions for making a protein called the common gamma chain. This protein is located on the surface of immature blood forming cells in bone… …   Wikipedia

  • Severe Combined Immunodeficiency — Klassifikation nach ICD 10 D81.0 SCID mit retikulärer Dysgenesie D81.1 SCID mit niedriger T und B Zellenzahl D81.2 …   Deutsch Wikipedia

  • severe combined immunodeficiency — noun a congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of life • Syn:… …   Useful english dictionary

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