Interstitial Cystitis

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

Interstitial cystitis, also known as bladder pain syndrome (IC/BPS), is a rare chronic debilitating urogenital disease characterized by urinary frequency, urgency, and pelvic pain.

Genes related to Interstitial Cystitis

CXCL9
CXCL11
CXCL10

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Interstitial Cystitis

Pain
Irritability
Abnormality of the genital system
Urinary urgency
Abnormal vagina morphology
Chronic pain
Pollakisuria
Abnormality of the menstrual cycle
Abnormality of the urethra
Dyspareunia

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

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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

Interstitial Cystitis Is also known as interstitial cystitis/bladder pain syndrome, bladder pain syndrome, ic/pbs, painful bladder syndrome, interstitial cystitis/painful bladder syndrome, ic/bps.

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.

Interstitial Cystitis Recommended genes panels

Panel Name, Specifity and genes Tested/covered
CXCL9. By Fulgent Genetics Fulgent Genetics (United States). CXCL9 Specificity 100 % Genes 34 %
CXCL11. By Fulgent Genetics Fulgent Genetics (United States). CXCL11 Specificity 100 % Genes 34 %
CXCL10. By Fulgent Genetics Fulgent Genetics (United States). CXCL10 Specificity 100 % Genes 34 %
Immune Report Card. By OmniSeq, Inc. (United States). CXCL10, STAT1, TBX21, TGFB1, TNF, TNFRSF14, TNFRSF18, CD40, CD27, TNFRSF9, TNFSF4, CD40LG, CCR2, CD163, CD2, CD28, CXCR6, CD38, CD4, CD68 , (...) View the complete list with 24 more genes Panel complete gene list CXCL10, STAT1, TBX21, TGFB1, TNF, TNFRSF14, TNFRSF18, CD40, CD27, TNFRSF9, TNFSF4, CD40LG, CCR2, CD163, CD2, CD28, CXCR6, CD38, CD4, CD68, CD80, CD86, CD8A, ICOSLG, CD244, HAVCR2, PDCD1LG2, DDX58, BTLA, CSF1R, CTLA4, ADORA2A, VSIR, GZMB, ICOS, IFNG, IL10, IL1B, IDO1, FOXP3, KLRD1, LAG3, MS4A1, MX1 Specificity 3 % Genes 34 %

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Sources and references

You can check the following sources for additional information.

MESH ORPHANET Rare Disease Symptoms Checker

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