CELIAC9
MCID: CLC042
MIFTS: 14

Celiac Disease 9 (CELIAC9)

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

Aliases & Classifications for Celiac Disease 9

MalaCards integrated aliases for Celiac Disease 9:

Name: Celiac Disease 9 57
Celiac Disease, Susceptibility to, 9 57 13
Gluten-Sensitive Enteropathy, Susceptibility to, 9 57
Gluten-Sensitive Enteropathy 9 57
Celiac9 57

Classifications:



External Ids:

OMIM® 57 612007
OMIM Phenotypic Series 57 PS212750
MedGen 41 C2677605

Summaries for Celiac Disease 9

OMIM® : 57 Celiac disease, also known as celiac sprue and gluten-sensitive enteropathy, is a multifactorial disorder of the small intestine that is influenced by both environmental and genetic factors. It is characterized by malabsorption resulting from inflammatory injury to the mucosa of the small intestine after the ingestion of wheat gluten or related rye and barley proteins (summary by Farrell and Kelly, 2002). For additional information and a discussion of genetic heterogeneity of celiac disease, see 212750. (612007) (Updated 20-May-2021)

MalaCards based summary : Celiac Disease 9, is also known as celiac disease, susceptibility to, 9. An important gene associated with Celiac Disease 9 is CELIAC9 (Celiac Disease, Susceptibility To, 9). Affiliated tissues include small intestine.

Related Diseases for Celiac Disease 9

Symptoms & Phenotypes for Celiac Disease 9

Clinical features from OMIM®:

612007 (Updated 20-May-2021)

Drugs & Therapeutics for Celiac Disease 9

Search Clinical Trials , NIH Clinical Center for Celiac Disease 9

Genetic Tests for Celiac Disease 9

Anatomical Context for Celiac Disease 9

MalaCards organs/tissues related to Celiac Disease 9:

40
Small Intestine

Publications for Celiac Disease 9

Articles related to Celiac Disease 9:

(show all 12)
# Title Authors PMID Year
1
Association of IL18RAP and CCR3 with coeliac disease in the Spanish population. 57
19542083 2009
2
Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease. 57
18805825 2009
3
Newly identified genetic risk variants for celiac disease related to the immune response. 57
18311140 2008
4
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. 57
17558408 2007
5
Celiac sprue. 57
11796853 2002
6
Utility of testing patients, on presentation, for serologic features of celiac disease. 61
24262940 2014
7
Clinical profile of coexisting conditions in type 1 diabetes mellitus patients. 61
23153973 2012
8
A prospective study of duodenal bulb biopsy in newly diagnosed and established adult celiac disease. 61
21606978 2011
9
[Plasma citrulline as a marker of loss of enterocitary mass in coeliac disease in childhood]. 61
22470028 2011
10
Expression of cyclin A in intestinal biopsies from children with celiac disease. 61
18999879 2008
11
Etiological spectrum of sporadic malabsorption syndrome in northern Indian adults at a tertiary hospital. 61
15250566 2004
12
Steatorrhea, a simple and rapid method of diagnosis. 61
939233 1976

Variations for Celiac Disease 9

Expression for Celiac Disease 9

Search GEO for disease gene expression data for Celiac Disease 9.

Pathways for Celiac Disease 9

GO Terms for Celiac Disease 9

Sources for Celiac Disease 9

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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