MYASTHENIA GRAVIS
General Information (adopted from Orphanet):
Synonyms, Signs: |
MG |
Number of Symptoms | 16 |
OrphanetNr: | |
OMIM Id: |
254200
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ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
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Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0010628) | Facial palsy | 146 / 7739 | ||||
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(HPO:0000508) | Ptosis | 459 / 7739 | ||||
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(HPO:0000651) | Diplopia | 37 / 7739 | ||||
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(HPO:0003473) | Fatigable weakness | 39 / 7739 | ||||
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(HPO:0002015) | Dysphagia | 301 / 7739 | ||||
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(HPO:0001260) | Dysarthria | 329 / 7739 | ||||
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(HPO:0005216) | Chewing difficulties | 6 / 7739 | ||||
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(HPO:0000836) | Hyperthyroidism | 25 / 7739 | ||||
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(HPO:0001611) | Nasal speech | 48 / 7739 | ||||
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(HPO:0100522) | Thymoma | 5 / 7739 | ||||
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(HPO:0002960) | Autoimmunity | 78 / 7739 | ||||
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(HPO:0003690) | Limb muscle weakness | 41 / 7739 | ||||
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(HPO:0003701) | Proximal muscle weakness | 105 / 7739 | ||||
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(OMIM) | Association with Gm type | 1 / 7739 | ||||
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(OMIM) | Antibodies to acetylcholine receptor (AChR) | 1 / 7739 | ||||
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(OMIM) | Ventilatory insufficiency | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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