Immunodeficiency 39; Imd39
Table of contents:
Clinical Features
Phenotypes and symptoms related to Immunodeficiency 39; Imd39
- Respiratory distress
- 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.Immunodeficiency 39; Imd39 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
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 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like USHER SYNDROME, TYPE IIIB; USH3B COFFIN-SIRIS SYNDROME 2; CSS2 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If; CDG1F AUTOSOMAL RECESSIVE CUTIS LAXA TYPE 2, CLASSIC TYPE CUSHING DISEASE SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13 JOUBERT SYNDROME 31; JBTS31