Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	GRAVES DISEASE, SUSCEPTIBILITY TO, 1
Synonyms	GRD
ID	http://purl.bioontology.org/ontology/OMIM/275000
altLabel	GRD THYROTOXICOSIS GRD1 HYPERTHYROIDISM, AUTOIMMUNE
cui	C0040156 C0018213 C1848795
Gene Locus	14q31
Gene Symbol	GRD1
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	275000
OMIM Entry Type	5
OMIM MimType Value	perc
prefLabel	GRAVES DISEASE, SUSCEPTIBILITY TO, 1
tui	T033 T047

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Mapping To	Ontology	Source
http://purl.bmicc.cn/ontology/ICD10CN/E05.9	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/MESH/D006111	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10/E05.9	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/LNC/LA14302-6	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0018213	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0040156	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/MESH/D013971	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10CM/E05.9	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10CM/E05.0	International Classification of Diseases, Version 10 - Clinical Modification	CUI