Mildly elevated creatine phosphokinase
Symptom Information:
Symptom ID: | HPO:0008180 | |||||||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of circulating protein level(HPO:0010876) Abnormality of circulating enzyme level(HPO:0011021) Elevated serum creatine phosphokinase(HPO:0003236) Mildly elevated creatine phosphokinase(HPO:0008180) MedDRA: |
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Database Frequency: | 28 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Congenital myasthenic syndromes with glycosylation defect | (Orphanet:353327) |
Distal myopathy with posterior leg and anterior hand involvement | (Orphanet:63273) |
Distal myopathy, Welander type | (Orphanet:603) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 | (OMIM:600969) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 | (OMIM:615424) |
Laing distal myopathy | (Orphanet:59135) |
MERRF | (Orphanet:551) |
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE | (OMIM:159400) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 12 | (OMIM:610542) |
MYASTHENIC SYNDROME, CONGENITAL, 14 | (OMIM:616228) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
Myasthenia gravis | (Orphanet:589) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
Perrault Syndrome 5 | (OMIM:616138) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
SATOYOSHI SYNDROME | (OMIM:600705) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |