Preferred Name |
Myasthenia Gravis |
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Synonyms |
Myasthenia gravis paralytica |
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Definitions |
A disorder of neuromuscular transmission characterized by weakness of cranial and skeletal muscles. Autoantibodies directed against acetylcholine receptors damage the motor endplate portion of the NEUROMUSCULAR JUNCTION, impairing the transmission of impulses to skeletal muscles. Clinical manifestations may include diplopia, ptosis, and weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles. THYMOMA is commonly associated with thi (source : MSH) |
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ID |
http://doe-generated-ontology.com/OntoAD#C0026896 |
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altLabel |
Myasthenia gravis paralytica Myasthénie grave pseudo-paralytique Goldflam-Erb Myasthénie auto-immune Myasthénie autoimmune paralysie bulbaire asthénique Myasthénie grave MG Myasthenia gravis syndrome d'Erb-Goldflam Erb-Goldflam disease Erb-Goldflam syndrome |
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contraindicated_drug | ||
definition |
A disorder of neuromuscular transmission characterized by weakness of cranial and skeletal muscles. Autoantibodies directed against acetylcholine receptors damage the motor endplate portion of the NEUROMUSCULAR JUNCTION, impairing the transmission of impulses to skeletal muscles. Clinical manifestations may include diplopia, ptosis, and weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles. THYMOMA is commonly associated with thi (source : MSH) |
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due_to | ||
has_manifestation | ||
has_severity | ||
hiddenLabel |
Myasthénie MyastheniaGravis |
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prefixIRI |
OntoAD:C0026896 |
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prefLabel |
Myasthénie Myasthenia Gravis |
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subClassOf |
http://doe-generated-ontology.com/OntoAD#C0004364 http://doe-generated-ontology.com/OntoAD#C1533847 http://doe-generated-ontology.com/OntoAD#C1285168 |