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

MERRF syndrome
Synonyms

Myoclonic epilepsy associated with ragged-red fibers
ID

http://purl.bioontology.org/ontology/ICD10CM/E88.42
altLabel

Myoclonic epilepsy associated with ragged-red fibers
CODE ALSO

progressive myoclonic epilepsy (G40.3-)
cui

C0162672
notation

E88.42
Order number

04969
prefLabel

MERRF syndrome
tui

T047
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/E88.4
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_310 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/MESH/D017243 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D017243 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/OMIM/516005 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.obolibrary.org/obo/MONDO_0010790 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0010790 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/590060 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/590050 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/590070 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/545000 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI