Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Jump to:
Spinner 000000 16px loading...
Preferred Name

Primary congenital glaucoma
ID

http://purl.obolibrary.org/obo/HP_0008007
database_cross_reference

UMLS:C1533041

SNOMEDCT_US:415176004
has_obo_namespace

human_phenotype
id

HP:0008007
label

Primary congenital glaucoma
notation

HP:0008007
prefLabel

Primary congenital glaucoma
treeView

http://purl.obolibrary.org/obo/HP_0001087
subClassOf

http://purl.obolibrary.org/obo/HP_0001087
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU073627 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/9C61.40 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.obolibrary.org/obo/DOID_0050593 Human Disease Ontology / 人类疾病本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C150251 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/MONDO_0000365 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0000365 Experimental Factor Ontology / 实验性因素本体 LOOM