Human Disease Ontology / 人类疾病本体

Last uploaded: September 7, 2023

Preferred Name	amelogenesis imperfecta
Definitions	Xref MGI. A dental enamel hypoplasia characterized by abnormal enamel formation.
ID	http://purl.obolibrary.org/obo/DOID_2187
comment	Xref MGI.
database_cross_reference	SNOMEDCT_US_2022_09_01:78494001 GARD:5791 ORDO:88661 ICD10CM:K00.5 OMIM:PS104500 MESH:D000567 UMLS_CUI:C0002452
definition	A dental enamel hypoplasia characterized by abnormal enamel formation.
has_obo_namespace	disease_ontology
id	DOID:2187
in_subset	http://purl.obolibrary.org/obo/doid#DO_rare_slim
label	amelogenesis imperfecta
notation	DOID:2187
prefLabel	amelogenesis imperfecta
subClassOf	http://purl.obolibrary.org/obo/DOID_693

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/D000567	Medical Subject Headings / 医学主题词表	LOOM
http://purl.obolibrary.org/obo/DOID_2187	BioAssay Ontology / 生物活性分析本体	LOOM
http://purl.obolibrary.org/obo/DOID_2187	BioAssay Ontology / 生物活性分析本体	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019507	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0019507	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037342	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://purl.obolibrary.org/obo/HP_0000705	Human Phenotype Ontology / 人类表型本体	LOOM
http://www.orpha.net/ORDO/Orphanet_88661	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/LA30.6	《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China	LOOM