Inflammatory Bowel Disease 13; Ibd13

Clinical Features

Phenotypes and symptoms related to Inflammatory Bowel Disease 13; Ibd13

  • Inflammation of the large intestine

Incidence and onset information

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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Inflammatory Bowel Disease 13; Ibd13 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
NGS Epilepsy/Seizure Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

SCN1A, SCN1B, SCN2A, SCN5A, SCN8A, SCN9A, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SLC2A1, SLC35A2, SLC9A6, SNAP25, SPTAN1, CDKL5, STXBP1, SYN1, SYNGAP1 , (...)

View the complete list with 124 more genes
Specificity
1 %
Genes
100 %
Colchicine resistance (sequence analysis of ABCB1 gene).

By CGC Genetics (Portugal).

ABCB1
Specificity
100 %
Genes
100 %
Colchicine resistance.

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

ABCB1
Specificity
100 %
Genes
100 %
Inflammatory bowel disease type 13.

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

ABCB1
Specificity
100 %
Genes
100 %
Pharmacogenetic panel.

By bio.logis Center for Human Genetics Diagnosticum (Germany).

SLC19A1, SLCO1B1, SOD2, TPMT, UGT1A1, CCR5, VKORC1, ADH1B, CYP2B6, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5, ADRB3, DPYD, ABCB1, G6PD, MTHFR, NAT2 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
100 %
MDR1.

By MVZ Dortmund Dr. Eberhard & Partner (Germany).

ABCB1
Specificity
100 %
Genes
100 %
Cardiovascular Diseases_General Panel.

By Health in Code (Spain).

RIT1, MRPL3, RRAS, RYR1, RYR2, SAR1B, BLK, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SDHA, BMPR1A, BMPR1B, BMPR2, SGCA, SGCB, SGCD , (...)

View the complete list with 351 more genes
Specificity
1 %
Genes
100 %
Dyslipidemias / Early atherosclerosis.

By Health in Code (Spain).

RYR1, SAR1B, BLK, SLCO1B1, SLC22A8, SLC2A2, HNF1A, HNF1B, KLF11, WFS1, ZMPSTE24, NEUROG3, ABCG5, ABCG8, LMF1, PCDH15, CAV1, BSCL2, SCARB1, TRIB1 , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
100 %

We have 11 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PTOSIS, HEREDITARY CONGENITAL 1; PTOS1 PROTEUS SYNDROME TSH-SECRETING PITUITARY ADENOMA CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1 EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS; TIIAC TYROSINEMIA, TYPE I; TYRSN1

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