Disease #01697 (CELIAC1 (celiac disease, susceptibility to, type 1 (CELIAC-1)), OMIM:212750)

Official abbreviation CELIAC1
Name celiac disease, susceptibility to, type 1 (CELIAC-1)
OMIM ID 212750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive, Multifactorial
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes HLA-DQA1, HLA-DQB1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00409554 K6694 PubMed: Oishi 2018 - F - Japan - - - - - CELIAC1 best corrected visual acuity: 0.3; electroretinogram , rod: non- recordable, cone: severely reduced CYP4V2 CYP4V2 1 1 LOVD
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