Complement Component 7 Deficiency; C7d

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 7 Deficiency; C7d

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Complement Component 7 Deficiency; C7d

Fever
Arthritis
Telangiectasia
Meningitis
Vasculitis
Raynaud phenomenon
Complement deficiency
Pyoderma
Sclerodactyly
Vasculitis in the skin

And another 5 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

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 7 Deficiency; C7d Is also known as c7 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 7 Deficiency; C7d Recommended genes panels

Panel Name, Specifity and genes Tested/covered
C7 Deletion/duplication analysis. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). C7 Specificity 100 % Genes 100 %
C7 Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). C7 Specificity 100 % Genes 100 %
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 %
C7. By Fulgent Genetics Fulgent Genetics (United States). C7 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 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Search Engine

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