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Ontology Browser

glycogen storage disease V (DOID:2746)
Annotations: Rat: (3) Mouse: (3) Human: (3) Chinchilla: (1) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
congenital disorder of glycosylation It  
Danon disease  
Glycogen Storage Disease 0, Liver  
Glycogen Storage Disease 0, Muscle  
glycogen storage disease I +   
glycogen storage disease II +   
glycogen storage disease III +   
glycogen storage disease IV +   
glycogen storage disease IX +   
glycogen storage disease V  
Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
glycogen storage disease VI  
glycogen storage disease VII  
glycogen storage disease VIII 
Glycogen Storage Disease XI  
Glycogen Storage Disease XII  
Glycogen Storage Disease XIII  
glycogen storage disease XV  
lethal congenital glycogen storage disease of heart  
Polyglucosan Body Disease, Adult Form  
Polyglucosan Body Myopathy 1 with or without Immunodeficiency  
Polyglucosan Body Myopathy 2  

Exact Synonyms: GSD V ;   GSD5 ;   Glycogen Storage Disease Type 5 ;   Glycogenosis 5 ;   McArdle Disease ;   McArdle Type Glycogen Storage Disease ;   McArdle syndromes ;   McArdle's Disease ;   McArdles Disease ;   Mcardle Syndrome ;   Muscle Glycogen Phosphorylase Deficiency ;   Muscle Phosphorylase Deficiencies ;   Muscle Phosphorylase Deficiency ;   Myophosphorylase deficiencies ;   Myophosphorylase deficiency ;   PYGM Deficiencies ;   PYGM deficiency ;   glycogen storage disease type V
Primary IDs: MESH:D006012
Alternate IDs: OMIM:232600
Xrefs: GARD:6528 ;   ICD10CM:E74.04 ;   NCI:C84738 ;   ORDO:368
Definition Sources: MESH:D006012

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.