Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Pseudohypoparathyroidism
ID	http://purl.bioontology.org/ontology/OMIM/MTHU005113
cui	C0033806
Manifestation of	http://purl.bioontology.org/ontology/OMIM/603233 http://purl.bioontology.org/ontology/OMIM/612462 http://purl.bioontology.org/ontology/OMIM/203330 http://purl.bioontology.org/ontology/OMIM/103580
notation	MTHU005113
prefLabel	Pseudohypoparathyroidism
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000131

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99027	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/ICD10CM/E20.1	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10CM/E20.1	International Classification of Diseases, Version 10 - Clinical Modification	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/5A50.1	International Classification of Diseases, 11th Edition, China	LOOM
http://purl.bioontology.org/ontology/MESH/D011547	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D011547	Medical Subject Headings	LOOM
http://purl.obolibrary.org/obo/DOID_4184	Human Disease Ontology 123	LOOM
http://purl.bmicc.cn/ontology/ICD10CN/E20.1	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10/E20.1	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/ICD10/E20.1	International Classification of Diseases, Version 10	LOOM