Human Disease Ontology / 人类疾病本体

Last uploaded: September 7, 2023

Preferred Name	gait apraxia
ID	http://purl.obolibrary.org/obo/DOID_4260
database_cross_reference	UMLS_CUI:C1510417 SNOMEDCT_US_2022_09_01:30767006 MESH:D020235
has exact match	MESH:D020235
has_obo_namespace	disease_ontology
id	DOID:4260
label	gait apraxia
notation	DOID:4260
prefLabel	gait apraxia
subClassOf	http://purl.obolibrary.org/obo/DOID_0060135

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/D020235	Medical Subject Headings / 医学主题词表	LOOM
http://purl.obolibrary.org/obo/DOID_4260	BioAssay Ontology / 生物活性分析本体	LOOM
http://purl.obolibrary.org/obo/DOID_4260	BioAssay Ontology / 生物活性分析本体	SAME_URI
http://purl.obolibrary.org/obo/HP_0010521	Human Phenotype Ontology / 人类表型本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0006766	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU006926	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://www.ebi.ac.uk/efo/EFO_1000944	Experimental Factor Ontology / 实验性因素本体	LOOM