Human Phenotype Ontology

Last uploaded: February 24, 2022
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Preferred Name

Spondylometaphyseal dysplasia
ID

http://purl.obolibrary.org/obo/HP_0002657
database_cross_reference

UMLS:C0700635

SNOMEDCT_US:702350003

MSH:C537501
has_obo_namespace

human_phenotype
id

HP:0002657
label

Spondylometaphyseal dysplasia
notation

HP:0002657
prefLabel

Spondylometaphyseal dysplasia
treeView

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

http://purl.obolibrary.org/obo/HP_0002652
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http://purl.obolibrary.org/obo/DOID_0112295 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU002631 Online Mendelian Inheritance in Man LOOM