Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Preferred Name

Spondyloepimetaphyseal dysplasia

ID

http://purl.obolibrary.org/obo/HP_0002651

database_cross_reference

SNOMEDCT_US:254062008

UMLS:C0432211

has_obo_namespace

human_phenotype

id

HP:0002651

label

Spondyloepimetaphyseal dysplasia

notation

HP:0002651

prefLabel

Spondyloepimetaphyseal dysplasia

treeView

http://purl.obolibrary.org/obo/HP_0002652

subClassOf

http://purl.obolibrary.org/obo/HP_0002652

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU005067 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/DOID_0080027 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_0080027 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0100510 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0100510 Experimental Factor Ontology / 实验性因素本体 LOOM