Easy fatigability
Symptom Information:
Symptom ID: | HPO:0003388 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Functional motor problems(HPO:0004302) Easy fatigability(HPO:0003388) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Easy fatigability(HPO:0003388) MedDRA: |
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Database Frequency: | 34 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant centronuclear myopathy | (Orphanet:169189) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Barth syndrome | (Orphanet:111) |
Camurati-Engelmann disease | (Orphanet:1328) |
Carnitine uptake deficiency | (Orphanet:158) |
Congenital myasthenic syndromes with glycosylation defect | (Orphanet:353327) |
Fabry disease | (Orphanet:324) |
Hurler-Scheie syndrome | (Orphanet:93476) |
MELAS | (Orphanet:550) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616326) |
MYASTHENIC SYNDROME, CONGENITAL, 12 | (OMIM:610542) |
MYASTHENIC SYNDROME, CONGENITAL, 16 | (OMIM:614198) |
MYASTHENIC SYNDROME, CONGENITAL, 18 | (OMIM:616330) |
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL | (OMIM:616313) |
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL | (OMIM:616321) |
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL | (OMIM:616322) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL | (OMIM:616324) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
MYASTHENIC SYNDROME, CONGENITAL, 8 | (OMIM:615120) |
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616325) |
MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES | (OMIM:616231) |
MYXEDEMA | (OMIM:255900) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Neutral lipid storage myopathy | (Orphanet:98908) |
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:265400) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
Tubular aggregate myopathy | (Orphanet:2593) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |