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Preferred Name

Dravet syndrome
Synonyms

Severe myoclonic epilepsy in infancy (SMEI)
ID

http://purl.bioontology.org/ontology/ICD10CM/G40.83
altLabel

Severe myoclonic epilepsy in infancy (SMEI)

Polymorphic epilepsy in infancy (PMEI)
cui

C5385212

C0751122
notation

G40.83
Order number

06316
prefLabel

Dravet syndrome
tui

T047
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/G40.8
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http://purl.obolibrary.org/obo/MONDO_0100135 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116573 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://www.orpha.net/ORDO/Orphanet_33069 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_33069 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/DOID_0080422 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_0080422 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/MESH/D004831 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/OMIM/607208 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/607208 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/8A61.11 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/OMIM/182389 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI