Human Disease Ontology / 人类疾病本体

Last uploaded: September 7, 2023

Preferred Name	pseudohypoparathyroidism
Definitions	OMIM mapping confirmed by DO. [SN].
ID	http://purl.obolibrary.org/obo/DOID_4184
comment	OMIM mapping confirmed by DO. [SN].
database_cross_reference	GARD:10758 UMLS_CUI:C0033806 SNOMEDCT_US_2022_09_01:190867002 NCI:C99027 MESH:D011547 ICD10CM:E20.1 OMIM:612462
has exact match	MESH:D011547
has_obo_namespace	disease_ontology
id	DOID:4184
in_subset	http://purl.obolibrary.org/obo/doid#DO_rare_slim http://purl.obolibrary.org/obo/doid#NCIthesaurus
label	pseudohypoparathyroidism
notation	DOID:4184
prefLabel	pseudohypoparathyroidism
subClassOf	http://purl.obolibrary.org/obo/DOID_896

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0019992	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0019992	Experimental Factor Ontology / 实验性因素本体	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99027	National Cancer Institute Thesaurus / 美国国家癌症研究所词典	LOOM
http://purl.bioontology.org/ontology/ICD10CM/E20.1	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/5A50.1	《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China	LOOM
http://purl.bioontology.org/ontology/MESH/D011547	Medical Subject Headings / 医学主题词表	LOOM
http://www.orpha.net/ORDO/Orphanet_97593	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.obolibrary.org/obo/DOID_4184	BioAssay Ontology / 生物活性分析本体	LOOM
http://purl.obolibrary.org/obo/DOID_4184	BioAssay Ontology / 生物活性分析本体	SAME_URI
http://purl.bioontology.org/ontology/OMIM/MTHU005113	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://purl.bioontology.org/ontology/ICD10/E20.1	International Classification of Diseases, Version 10 / 《国际疾病分类》第10版	LOOM
http://purl.obolibrary.org/obo/HP_0000852	Human Phenotype Ontology / 人类表型本体	LOOM