Invasive Pneumococcal Disease, Recurrent Isolated, 2; Ipd2
Genes related to Invasive Pneumococcal Disease, Recurrent Isolated, 2; Ipd2
- IKBKG
Clinical Features
Top most frequent phenotypes and symptoms related to Invasive Pneumococcal Disease, Recurrent Isolated, 2; Ipd2
- Fever
- Frontal bossing
- Hyperhidrosis
- Arthritis
- Dry skin
- Hypodontia
- Ectodermal dysplasia
- Osteomyelitis
- Cellulitis
- Periorbital edema
And another 2 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.
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.Invasive Pneumococcal Disease, Recurrent Isolated, 2; Ipd2 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
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![]() By Baylor Miraca Genetics Laboratories (United States).
IKBKG
Specificity
100 %
Genes
100 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
IKBKG
Specificity
100 %
Genes
100 % |
![]() By Molecular Diagnostic Laboratory University of Alberta (Canada).
IKBKG
Specificity
100 %
Genes
100 % |
![]() By Molecular Diagnostic Laboratory University of Alberta (Canada).
IKBKG
Specificity
100 %
Genes
100 % |
![]() By ARUP Laboratories, Molecular Genetics and Genomics (United States).
SH2D1A, BTK, CD40, CD40LG, UNG, VAV1, AICDA, BLNK, CD19, CD79A, CD79B, CD81, LRBA, TNFRSF13C, TNFRSF13B, ADA, LRRC8A, CR2, ICOS, IGHM , (...)
View the complete list with 15 more genes
Specificity
3 %
Genes
100 % |
![]() By GeneDx (United States).
IKBKG
Specificity
100 %
Genes
100 % |
![]() By GeneDx (United States).
IKBKG
Specificity
100 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
IKBKG
Specificity
100 %
Genes
100 % |
You can get up to 46 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 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10 NEPHROGENIC DIABETES INSIPIDUS MYOPATHY, MYOFIBRILLAR, 4; MFM4 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS2 BEHAVIORAL VARIANT OF FRONTOTEMPORAL DEMENTIA RETINITIS PIGMENTOSA 3; RP3