Fatigable weakness
Symptom Information:
Symptom ID: | HPO:0003473 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Abnormal synaptic transmission at the neuromuscular junction(HPO:0003398) Fatigable weakness(HPO:0003473) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Fatigable weakness(HPO:0003473) MedDRA: General disorders and administration site conditions(MedDRA:10018065) General system disorders NEC(MedDRA:10018073) Asthenic conditions(MedDRA:10003550) Fatigable weakness(HPO:0003473) |
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Database Frequency: | 39 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
CLUSTER HEADACHE, FAMILIAL | (OMIM:119915) |
Congenital myasthenic syndromes | (Orphanet:590) |
Congenital myasthenic syndromes with glycosylation defect | (Orphanet:353327) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cystinosis | (Orphanet:213) |
EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL | (OMIM:129840) |
Epidermolysis bullosa simplex with anodontia/hypodontia | (Orphanet:2325) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type | (Orphanet:79399) |
Good syndrome | (Orphanet:169105) |
Hemochromatosis type 3 | (Orphanet:225123) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MELAS | (Orphanet:550) |
MYASTHENIA GRAVIS | (OMIM:254200) |
MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE | (OMIM:159400) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 12 | (OMIM:610542) |
MYASTHENIC SYNDROME, CONGENITAL, 14 | (OMIM:616228) |
MYASTHENIC SYNDROME, CONGENITAL, 15 | (OMIM:616227) |
MYASTHENIC SYNDROME, CONGENITAL, 16 | (OMIM:614198) |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | (OMIM:601462) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
Menkes disease | (Orphanet:565) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Myasthenia gravis | (Orphanet:589) |
PGM1-CDG | (Orphanet:319646) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
Primary systemic amyloidosis | (Orphanet:314701) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
Thymic carcinoma | (Orphanet:99868) |
Thymic epithelial neoplasm | (Orphanet:3398) |
Thymic tumor | (Orphanet:100100) |
Thymoma | (Orphanet:99867) |