IBD21
MCID: INF080
MIFTS: 20

Inflammatory Bowel Disease 21 (IBD21)

Categories: Blood diseases, Bone diseases, Gastrointestinal diseases, Genetic diseases, Immune diseases, Rare diseases

Aliases & Classifications for Inflammatory Bowel Disease 21

MalaCards integrated aliases for Inflammatory Bowel Disease 21:

Name: Inflammatory Bowel Disease 21 57 12 13 15 70
Ibd21 57 12

Characteristics:

OMIM®:

57 (Updated 20-May-2021)
Inheritance:
autosomal dominant


HPO:

31
inflammatory bowel disease 21:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

Disease Ontology 12 DOID:0110906
OMIM® 57 612354
OMIM Phenotypic Series 57 PS266600
MedGen 41 C2676507
SNOMED-CT via HPO 68 263681008 64766004
UMLS 70 C2676507

Summaries for Inflammatory Bowel Disease 21

Disease Ontology : 12 An inflammatory bowel disease that has material basis in variation in the chromosome region 18p11.

MalaCards based summary : Inflammatory Bowel Disease 21, also known as ibd21, is related to inflammatory bowel disease and peliosis hepatis. An important gene associated with Inflammatory Bowel Disease 21 is IBD21 (Inflammatory Bowel Disease-21). Related phenotype is ulcerative colitis.

More information from OMIM: 612354 PS266600

Related Diseases for Inflammatory Bowel Disease 21

Symptoms & Phenotypes for Inflammatory Bowel Disease 21

Human phenotypes related to Inflammatory Bowel Disease 21:

31
# Description HPO Frequency HPO Source Accession
1 ulcerative colitis 31 HP:0100279

Symptoms via clinical synopsis from OMIM®:

57 (Updated 20-May-2021)
Abdomen Gastrointestinal:
ulcerative colitis
crohn disease

Clinical features from OMIM®:

612354 (Updated 20-May-2021)

Drugs & Therapeutics for Inflammatory Bowel Disease 21

Search Clinical Trials , NIH Clinical Center for Inflammatory Bowel Disease 21

Genetic Tests for Inflammatory Bowel Disease 21

Anatomical Context for Inflammatory Bowel Disease 21

Publications for Inflammatory Bowel Disease 21

Articles related to Inflammatory Bowel Disease 21:

(show all 12)
# Title Authors PMID Year
1
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 57
18587394 2008
2
Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis. 57
18438405 2008
3
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. 57
18438406 2008
4
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 57
17554261 2007
5
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 57
17554300 2007
6
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 57
17435756 2007
7
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. 57
17447842 2007
8
[Value of capsule endoscopy in children with small intestinal diseases with hematochezia as the chief complaint]. 61
32933635 2020
9
Readmission after colorectal surgery is related to preoperative clinical conditions and major complications. 61
23929019 2013
10
Efficacy and safety of pulse steroid therapy in Japanese pediatric patients with ulcerative colitis: a survey of the Japanese Society for Pediatric Inflammatory Bowel Disease. 61
20090334 2010
11
Coagulation factor XIII and markers of thrombin generation and fibrinolysis in patients with inflammatory bowel disease. 61
11953689 2002
12
Histopathological evaluation of colonic mucosal biopsy specimens in chronic inflammatory bowel disease: diagnostic implications. 61
1773958 1991

Variations for Inflammatory Bowel Disease 21

Expression for Inflammatory Bowel Disease 21

Search GEO for disease gene expression data for Inflammatory Bowel Disease 21.

Pathways for Inflammatory Bowel Disease 21

GO Terms for Inflammatory Bowel Disease 21

Sources for Inflammatory Bowel Disease 21

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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