Complement Component 4B Deficiency

Alternative Names

  • C4BD
  • C4B Deficiency

Associated Genes

Complement Component 4B
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WHO-ICD-10 version:2010

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Certain disorders involving the immune mechanism

OMIM Number

614379

Mode of Inheritance

Autosomal recessive

Gene Map Locus

6p21.33

Description

C4B deficiency is caused by mutation in the C4B gene. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
614379.1United Arab EmiratesFemaleYes Juvenile rheumatoid arthritis; Arthropa...NM_001002029.3:c.(?_3231)_(3387_?)delHomozygousAutosomal, RecessiveFathalla et al. 2021 Homozygous for an ex...
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