Complement Component 6 Deficiency; C6d
Table of contents:
Clinical Features
Phenotypes and symptoms related to Complement Component 6 Deficiency; C6d
- Meningitis
- Hemoglobinuria
- Complement deficiency
- Paroxysmal nocturnal hemoglobinuria
- Recurrent meningococcal disease
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Complement Component 6 Deficiency; C6d Is also known as c6 deficiency.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Complement Component 6 Deficiency; C6d Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Complement deficiencies Panel.
By CeGaT GmbH (Germany).
CFB, THBD, SERPING1, C1QA, C1QB, C1QC, C1R, C1S, C2, C3, C4A, C4B, C5, C6, C7, C8A, C8B, C8G, C9, CD59 , (...)
View the complete list with 14 more genes
Specificity
3 %
Genes
100 % |
C6.
By Fulgent Genetics Fulgent Genetics (United States).
C6
Specificity
100 %
Genes
100 % |
Complement System Disorder Panel.
By Blueprint Genetics (Finland).
CFB, SPAG1, THBD, SERPING1, RSPH1, C1QA, C1QB, C1QBP, C1QC, C1S, C2, VTN, C3, C3AR1, C4BPA, C4BPB, C5, C5AR1, C6, C7 , (...)
View the complete list with 55 more genes
Specificity
2 %
Genes
100 % |
You can get up to -5 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like WEBB-DATTANI SYNDROME; WEDAS IDIOPATHIC ACHALASIA C1q DEFICIENCY; C1QD MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY); MTDPS8A PEUTZ-JEGHERS SYNDROME; PJS VELOCARDIOFACIAL SYNDROME