Mondo Disease Ontology

Last uploaded: May 9, 2024

Preferred Name	hypothyroidism, congenital, nongoitrous
Synonyms
ID	http://purl.obolibrary.org/obo/MONDO_0000045
database_cross_reference	OMIMPS:275200
exactMatch	https://omim.org/phenotypicSeries/PS275200
IAO_0000233	https://github.com/monarch-initiative/mondo/issues/4069
id	MONDO:0000045
in_subset	http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare http://purl.obolibrary.org/obo/mondo#otar
label	hypothyroidism, congenital, nongoitrous
notation	MONDO:0000045
prefLabel	hypothyroidism, congenital, nongoitrous
treeView	http://purl.obolibrary.org/obo/MONDO_0018612 http://purl.obolibrary.org/obo/MONDO_0003847
subClassOf	http://purl.obolibrary.org/obo/MONDO_0018612 http://purl.obolibrary.org/obo/MONDO_0003847

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0000045	EFO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0000045	DOVES	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0000045	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0000045	DOVES	LOOM