Human Phenotype Ontology

Last uploaded: February 24, 2022
Preferred Name

Hypopituitarism

ID

http://purl.obolibrary.org/obo/HP_0040075

created_by

HPO:skoehler

database_cross_reference

SNOMEDCT_US:74728003

MSH:D007018

UMLS:C0020635

has_obo_namespace

human_phenotype

id

HP:0040075

label

Hypopituitarism

notation

HP:0040075

prefLabel

Hypopituitarism

treeView

http://purl.obolibrary.org/obo/HP_0011747

subClassOf

http://purl.obolibrary.org/obo/HP_0011747

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

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/E23.0 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU036880 Online Mendelian Inheritance in Man LOOM
http://purl.bmicc.cn/ontology/ICD11CN/5A61.0 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/MESH/D007018 Medical Subject Headings LOOM
http://purl.obolibrary.org/obo/DOID_9406 Human Disease Ontology 123 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C62591 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/ICD10/E23.0 International Classification of Diseases, Version 10 LOOM