Easy fatigability

Symptom Information:

Symptom ID: HPO:0003388
Synonyms:
Easy fatigability [OMIM:Easy fatigability]
Quality:
Cross references:
OMIM: "Easy fatigability" [OMIM:Easy fatigability]
Is a (Direct Parents):
HPO         Functional motor problems
HPO         Abnormality of nervous system physiology
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:
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)