Complement Component 7 Deficiency; C7d
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.
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
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
Specificity
2 %
Genes
100 % |
You can get up to -3 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; CLIFAHDD AORTIC VALVE DISEASE 1; AOVD1 AMYOTROPHY, HEREDITARY NEURALGIC; HNA BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1 CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP MESOTHELIOMA, MALIGNANT; MESOM DEAFNESS, AUTOSOMAL RECESSIVE 44; DFNB44