MYASTHENIA GRAVIS

General Information (adopted from Orphanet):

Synonyms, Signs: MG
Number of Symptoms 16
OrphanetNr:
OMIM Id: 254200
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0010628) Facial palsy 146 / 7739
2
 (HPO:0000508) Ptosis 459 / 7739
3
 (HPO:0000651) Diplopia 37 / 7739
4
 (HPO:0003473) Fatigable weakness 39 / 7739
5
 (HPO:0002015) Dysphagia 301 / 7739
6
 (HPO:0001260) Dysarthria 329 / 7739
7
 (HPO:0005216) Chewing difficulties 6 / 7739
8
 (HPO:0000836) Hyperthyroidism 25 / 7739
9
 (HPO:0001611) Nasal speech 48 / 7739
10
 (HPO:0100522) Thymoma 5 / 7739
11
 (HPO:0002960) Autoimmunity 78 / 7739
12
 (HPO:0003690) Limb muscle weakness 41 / 7739
13
 (HPO:0003701) Proximal muscle weakness 105 / 7739
14
 (OMIM) Association with Gm type 1 / 7739
15
 (OMIM) Antibodies to acetylcholine receptor (AChR) 1 / 7739
16
 (OMIM) Ventilatory insufficiency 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: