Immunodeficiency 37; Imd37

Clinical Features

Phenotypes and symptoms related to Immunodeficiency 37; Imd37

  • Seizures
  • Immunodeficiency
  • Recurrent infections
  • Respiratory tract infection
  • Decreased antibody level in blood
  • Status epilepticus
  • Progressive neurologic deterioration
  • Lymphopenia
  • Encephalitis
  • Combined immunodeficiency

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.


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Immunodeficiency 37; Imd37 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Mesothelioma, somatic.

By Centogene AG - the Rare Disease Company (Germany).

BCL10
Specificity
100 %
Genes
100 %
Lymphoma, MALT, somatic.

By Centogene AG - the Rare Disease Company (Germany).

BCL10
Specificity
100 %
Genes
100 %
Lymphoma, follicular, somatic.

By Centogene AG - the Rare Disease Company (Germany).

BCL10
Specificity
100 %
Genes
100 %
Male germ cell tumor, somatic.

By Centogene AG - the Rare Disease Company (Germany).

BCL10
Specificity
100 %
Genes
100 %
Invitae Comprehensive Severe Combined Immunodeficiency (SCID) and Combined Immunodeficiency (CID) Panel.

By Invitae (United States).

STK4, TAPBP, TNFRSF4, CD27, CD40LG, ZAP70, CARD11, CD3D, CD3E, CD3G, CD247, CD8A, LRBA, DCLRE1C, ADA, DOCK8, CORO1A, CTPS1, NHEJ1, MAGT1 , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
100 %
Invitae Primary Immunodeficiency Panel.

By Invitae (United States).

RMRP, RORC, SEMA3E, SH2D1A, SH3BP2, SLC7A7, SMARCAL1, BTK, STAT1, STAT2, STAT3, STAT5B, STIM1, STK4, STX11, STXBP2, TAPBP, TAZ, TBK1, TCN2 , (...)

View the complete list with 187 more genes
Specificity
1 %
Genes
100 %
Invitae Combined Immunodeficiency (CID) Panel.

By Invitae (United States).

STK4, TAPBP, TNFRSF4, CD27, CD40LG, ZAP70, CARD11, CD3G, CD8A, LRBA, DOCK8, CTPS1, MAGT1, DOCK2, TAP1, TAP2, ICOS, IKBKB, IL21, IL21R , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
100 %
BCL10.

By Fulgent Genetics Fulgent Genetics (United States).

BCL10
Specificity
100 %
Genes
100 %

We have 8 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

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