Phosphorylase kinase deficiency in heart muscle only
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Phosphorylase kinase deficiency in heart muscle only" [OMIM:Phosphorylase kinase deficiency in heart muscle only] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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2 / 7739
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Resource:
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All diseases associated with this symptom:
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Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease
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(Orphanet:439854)
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[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL
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(OMIM:261740)
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