Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

congenital myasthenic syndrome
Synonyms

myasthenia gravis congenital

myasthenia gravis pseudoparalytica

congenital myasthenia

familial limb-girdle myasthenia

erb-Goldflam syndrome

congenital MG

myasthenic syndrome, congenital

Congenital Myasthenic Syndromes

CMS

Definitions

Congenital myasthenic syndrome (CMS) is a group of genetic disorders of impaired neuromuscular transmission at the motor endplate characterized by fatigable muscle weakness.

ID

http://purl.obolibrary.org/obo/MONDO_0018940

database_cross_reference

OMIMPS:601462

ICD9:V17.89

Orphanet:590

NCIT:C84647

NANDO:1200021

ICD9:358.00

MESH:D020294

UMLS:C0751882

MEDGEN:155650

SCTID:230672006

icd11.foundation:1515367530

DOID:3635

GARD:11902

NORD:1893

definition

Congenital myasthenic syndrome (CMS) is a group of genetic disorders of impaired neuromuscular transmission at the motor endplate characterized by fatigable muscle weakness.

has_exact_synonym

myasthenic syndrome, congenital

Congenital Myasthenic Syndromes

CMS

has_related_synonym

myasthenia gravis congenital

myasthenia gravis pseudoparalytica

congenital myasthenia

familial limb-girdle myasthenia

erb-Goldflam syndrome

congenital MG

IAO_0000233

https://github.com/monarch-initiative/mondo/issues/6744

id

MONDO:0018940

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder

label

congenital myasthenic syndrome

notation

MONDO:0018940

preferred label

congenital myasthenic syndrome

prefLabel

congenital myasthenic syndrome

see also

https://rarediseases.info.nih.gov/diseases/11902/congenital-myasthenic-syndrome

skos_exactMatch

http://identifiers.org/snomedct/230672006

http://purl.obolibrary.org/obo/Orphanet_590

http://purl.obolibrary.org/obo/NCIT_C84647

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1515367530

http://linkedlifedata.com/resource/umls/id/C0751882

http://identifiers.org/medgen/155650

http://identifiers.org/mesh/D020294

https://omim.org/phenotypicSeries/PS601462

http://purl.obolibrary.org/obo/DOID_3635

subClassOf

http://purl.obolibrary.org/obo/MONDO_0020124

http://purl.obolibrary.org/obo/MONDO_0100546

http://purl.obolibrary.org/obo/MONDO_0002254

excluded_subClassOf

http://purl.obolibrary.org/obo/MONDO_0020260

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Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0018940 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018940 DOVES SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018940 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018940 MONDO LOOM
http://purl.obolibrary.org/obo/DOID_3635 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0018940 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0018940 EFO LOOM
http://nanbyodata.jp/ontology/NANDO_1200021 NANDO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/230672006 SNOMEDCT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Congenital_Myasthenic_Syndrome CSEO LOOM
http://purl.obolibrary.org/obo/NCIT_C84647 BERO LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12597 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12597 NIFSTD LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU068681 OMIM LOOM
http://www.orpha.net/ORDO/Orphanet_590 ORDO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_3635 NATPRO LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12597 BIRNLEX LOOM
http://purl.bioontology.org/ontology/MEDDRA/10083942 MEDDRA LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84647 NCIT LOOM
http://purl.obolibrary.org/obo/DOID_3635 DTO LOOM
http://purl.obolibrary.org/obo/DOID_3635 BAO LOOM
http://purl.obolibrary.org/obo/DOID_3635 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_3635 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_3635 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_3635 FNS-H LOOM