Normal serum creatine kinase
Symptom Information:
|
Symptom ID:
|
OMIM : No Id available
|
|
Synonyms:
|
|
|
Quality:
|
|
|
Cross references:
|
| OMIM: "Normal serum creatine kinase" [OMIM:Normal serum creatine kinase] |
|
|
Is a (Direct Parents):
|
|
|
Is a (Whole tree):
|
HPO:
MedDRA:
|
|
Database Frequency:
|
12 / 7739
|
|
Resource:
|
|
All diseases associated with this symptom:
|
Congenital lethal myopathy, Compton-North type
|
(Orphanet:210163)
|
|
Congenital multicore myopathy with external ophthalmoplegia
|
(Orphanet:98905)
|
|
Congenital myopathy with internal nuclei and atypical cores
|
(Orphanet:319160)
|
|
Distal arthrogryposis type 10
|
(Orphanet:251515)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
|
(Orphanet:308712)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
|
(Orphanet:308684)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
|
(Orphanet:308698)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
|
(Orphanet:308670)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
|
(Orphanet:308655)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
|
(Orphanet:308638)
|
|
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
|
(Orphanet:308621)
|
|
Hereditary myoclonus - progressive distal muscular atrophy
|
(Orphanet:2590)
|