Preferred Name

Attention Deficit Hyperactivity Disorder

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97160

ALT_DEFINITION

A neurodevelopmental disorder presenting in early childhood that is characterized by chronic and excessive inattention, overactivity, and/or impulsivity.

code

C97160

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97150

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C189762

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

Contributing_Source

MedDRA

NICHD

Cellosaurus

DEFINITION

A disorder characterized by a marked pattern of inattention and/or hyperactivity-impulsivity that is inconsistent with developmental level and clearly interferes with functioning in at least two settings (e.g. at home and at school). When present, the symptoms of hyperactivity are most often present before the age of 7 years. There are three recognized presentations or subtypes from most to least common: combined type, inattentive/distractible type, hyperactive/impulsive type.

FULL_SYN

ADHD

Attention Deficit-Hyperactivity Disorder

Attention Deficit Hyperactivity Disorder

Attention Deficit/Hyperactivity Disorder

label

Attention Deficit Hyperactivity Disorder

Maps_To

Attention deficit/hyperactivity disorder

Preferred_Name

Attention Deficit Hyperactivity Disorder

prefixIRI

Thesaurus:C97160

prefLabel

Attention Deficit Hyperactivity Disorder

Semantic_Type

Mental or Behavioral Dysfunction

UMLS_CUI

C4230171

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2893

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/143465 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/MONDO_0007743 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/DOID_1094 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_1094 Human Disease Ontology / 人类疾病本体 LOOM
http://www.ebi.ac.uk/efo/EFO_0003888 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU031256 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU065489 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU062858 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU045734 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0007018 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU022819 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/6A05 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM