Mildly elevated creatine phosphokinase

Symptom Information:

Symptom ID: HPO:0008180
Synonyms:
Mildly increased creatine kinase [HPO:0008180]
Mildly increased serum creatine kinase [HPO:0008180]
Moderately increased serum creatine kinase [HPO:0008180]
Mildly increased creatine kinase [OMIM:Mildly increased creatine kinase]
Mildly increased serum creatine kinase [OMIM:Mildly increased serum creatine kinase]
Moderately increased serum creatine kinase [OMIM:Moderately increased serum creatine kinase]
Mildly elevated creatine phosphokinase (CPK) (120270.0002) [OMIM:Mildly elevated creatine phosphokinase (CPK) (120270.0002)]
Quality:
Cross references:
OMIM: "Mildly increased creatine kinase" [OMIM:Mildly increased creatine kinase]
OMIM: "Mildly increased serum creatine kinase" [OMIM:Mildly increased serum creatine kinase]
OMIM: "Moderately increased serum creatine kinase" [OMIM:Moderately increased serum creatine kinase]
OMIM: "Mildly elevated creatine phosphokinase (CPK) (120270.0002)" [OMIM:Mildly elevated creatine phosphokinase (CPK) (120270.0002)]
Is a (Direct Parents):
HPO         Elevated serum creatine phosphokinase
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:
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)