Complement Component 9 Deficiency; C9d

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Complement Component 9 Deficiency; C9d

Clinical Features

Phenotypes and symptoms related to Complement Component 9 Deficiency; C9d

Neoplasm
Jaundice
Stomach cancer
Hemoglobinuria
Complement deficiency
Paroxysmal nocturnal hemoglobinuria
Decreased serum complement C9

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 9 Deficiency; C9d Is also known as c9 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 9 Deficiency; C9d 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 Panel complete gene list CFB, THBD, SERPING1, C1QA, C1QB, C1QC, C1R, C1S, C2, C3, C4A, C4B, C5, C6, C7, C8A, C8B, C8G, C9, CD59, CFHR3, COLEC11, CFD, DGKE, FCN3, CFH, CFHR1, CFI, ITGB2, MASP1, MASP2, CD46, CFP, PIGA Specificity 3 % Genes 100 %
C9. By Fulgent Genetics Fulgent Genetics (United States). C9 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 Panel complete gene list CFB, SPAG1, THBD, SERPING1, RSPH1, C1QA, C1QB, C1QBP, C1QC, C1S, C2, VTN, C3, C3AR1, C4BPA, C4BPB, C5, C5AR1, C6, C7, C8A, C8B, C8G, C9, ADIPOQ, CD93, NME8, LRRC6, CD59, VSIG4, COLEC11, CCNO, DNAI2, HYDIN, ZMYND10, DNAAF2, CLU, RSPH9, DNAAF4, RSPH4A, DNAL1, CR2, CRP, ADIPOR1, ADIPOR2, DRC1, CCDC39, ARMC4, OFD1, DNAAF5, CCDC40, CCDC114, CD55, CFD, DGKE, DNAH11, DNAH5, DNAI1, CCDC65, DNAAF3, DNAAF1, CCDC103, FCN1, FCN2, FCN3, C5AR2, CFH, CFI, MASP1, MASP2, MAT2A, CD46, CFP, PIGA, PTX3 Specificity 2 % Genes 100 %
ATYPICAL HEMOLYTIC UREMIC SYNDROME: NGS PANEL. By Laboratorio de Genetica Clinica SL (Spain). CFB, THBD, C1S, C2, C3, C3AR1, C8A, C9, CFHR4, CFHR3, CR1, CR2, MMACHC, CFHR5, DGKE, F12, CFH, CFHR1, CFHR2, CFI , (...) View the complete list with 4 more genes Panel complete gene list CFB, THBD, C1S, C2, C3, C3AR1, C8A, C9, CFHR4, CFHR3, CR1, CR2, MMACHC, CFHR5, DGKE, F12, CFH, CFHR1, CFHR2, CFI, MASP1, CD46, PHB, PLG Specificity 5 % Genes 100 %
Macular Degeneration Related Disorders , Panel Massive Sequencing (NGS) 15 Genes. By Reference Laboratory Genetics (Spain). CFB, C2, C3, C9, RAX2, HMCN1, CST3, CX3CR1, ARMS2, ABCA4, ERCC6, FBLN5, CFH, CFI, HTRA1 Specificity 7 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

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