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EpilepsyOntology
Last uploaded:
November 8, 2021
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Preferred Name | myasthenia gravis | |
Synonyms |
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Definitions |
An autoimmune disease of the nervous system that has_material_basis_in antibodies to acetylcholine receptors at the neuromuscular junction, has_symptom ptosis, has_symptom diplopia, has_symptom dysphagia, has_symptom dysarthria, has_symptom muscle weakness and has_symptom dyspnea. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_437 |
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comment |
OMIM mapping confirmed by DO. [SN].
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database_cross_reference |
ICD10CM:G70.00 SNOMEDCT_US_2018_03_01:91637004 ICD10CM:G70.0 UMLS_CUI:C0026896 OMIM:254200 ICD9CM:358.0 ICD9CM:358.00 MESH:D009157 UMLS_CUI:C1260409 GARD:7122 NCI:C60989
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fromESSO |
true
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fromPubMed |
true
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has_alternative_id |
DOID:443 DOID:444
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has_obo_namespace |
disease_ontology
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hasDbXRef | ||
id |
DOID:437
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imported from | ||
in subset | ||
label |
myasthenia gravis
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notation |
DOID:437
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prefLabel |
myasthenia gravis
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文本定义 |
An autoimmune disease of the nervous system that has_material_basis_in antibodies to acetylcholine receptors at the neuromuscular junction, has_symptom ptosis, has_symptom diplopia, has_symptom dysphagia, has_symptom dysarthria, has_symptom muscle weakness and has_symptom dyspnea.
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subClassOf |
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