Human Phenotype Ontology

Last uploaded: July 1, 2024

Preferred Name	Abnormality of multiple cell lineages in the bone marrow
Synonyms
ID	http://purl.obolibrary.org/obo/HP_0012145
creation_date	2012-09-16T08:21:57Z
database_cross_reference	UMLS:C4023024
has_obo_namespace	human_phenotype
id	HP:0012145
label	Abnormality of multiple cell lineages in the bone marrow
notation	HP:0012145
prefLabel	Abnormality of multiple cell lineages in the bone marrow
terms_creator	https://orcid.org/0000-0002-0736-9199
treeView	http://purl.obolibrary.org/obo/HP_0005561
subClassOf	http://purl.obolibrary.org/obo/HP_0005561

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0012145	OBA	SAME_URI
http://purl.obolibrary.org/obo/HP_0012145	MAXO	SAME_URI
http://purl.obolibrary.org/obo/HP_0012145	UPHENO	SAME_URI
http://purl.obolibrary.org/obo/HP_0012145	KTAO	SAME_URI
http://purl.obolibrary.org/obo/HP_0012145	MAXO	LOOM
http://purl.obolibrary.org/obo/HP_0012145	OBA	LOOM
http://purl.obolibrary.org/obo/HP_0012145	UPHENO	LOOM
http://purl.obolibrary.org/obo/HP_0012145	KTAO	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00001139	PMAPP-PMO	LOOM