Jump to:
Spinner 000000 16px loading...
Preferred Name

Frontal encephalocele
ID

http://purl.bioontology.org/ontology/ICD10CM/Q01.0
cui

C0431289
notation

Q01.0
Order number

28779
prefLabel

Frontal encephalocele
tui

T019
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/Q01
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10/Q01.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10/Q01.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037938 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU037938 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/MESH/D004677 Medical Subject Headings / 医学主题词表 CUI
http://purl.obolibrary.org/obo/HP_0007330 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/Q01.0 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.obolibrary.org/obo/MONDO_0016020 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0016020 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU075885 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://www.orpha.net/ORDO/Orphanet_1931 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM