Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库

Last uploaded: September 7, 2023

Preferred Name	Congenital nystagmus
ID	http://purl.bioontology.org/ontology/OMIM/MTHU053438
cui	C0700501
Manifestation of	http://purl.bioontology.org/ontology/OMIM/145350 http://purl.bioontology.org/ontology/OMIM/136520 http://purl.bioontology.org/ontology/OMIM/620167
notation	MTHU053438
prefLabel	Congenital nystagmus
tui	T019
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000020

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_9649	BioAssay Ontology / 生物活性分析本体	LOOM
http://purl.obolibrary.org/obo/DOID_9649	Human Disease Ontology / 人类疾病本体	LOOM
http://purl.bioontology.org/ontology/MESH/D020417	Medical Subject Headings / 医学主题词表	CUI
http://www.ebi.ac.uk/efo/EFO_0007217	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.obolibrary.org/obo/HP_0006934	Human Phenotype Ontology / 人类表型本体	LOOM
http://purl.bioontology.org/ontology/ICD10CM/H55.01	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
http://purl.bioontology.org/ontology/ICD10CM/H55.01	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	LOOM
http://purl.obolibrary.org/obo/MONDO_0005712	Mondo Disease Ontology / Mondo疾病本体	LOOM