Increased hepatic glycogen content

Symptom Information:

Symptom ID: HPO:0006568
Synonyms:
Increased liver glycogen content [HPO:0006568]
Increased liver glycogen content [OMIM:Increased liver glycogen content]
Quality:
Cross references:
OMIM: "Increased liver glycogen content" [OMIM:Increased liver glycogen content]
Is a (Direct Parents):
HPO         Abnormality of the liver
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Increased hepatic glycogen content(HPO:0006568)
MedDRA:
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

3-hydroxy-3-methylglutaryl-CoA synthase deficiency (Orphanet:35701)
Alpha-mannosidosis (Orphanet:61)
Apolipoprotein A-I deficiency (Orphanet:425)
Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Aspartylglucosaminuria (Orphanet:93)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Congenital atransferrinemia (Orphanet:1195)
Congenital disorder of glycosylation (Orphanet:137)
Farber lipogranulomatosis (Orphanet:333)
Fucosidosis (Orphanet:349)
GAPO syndrome (Orphanet:2067)
GM1 gangliosidosis (Orphanet:354)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Glycogen storage disease due to liver glycogen phosphorylase deficiency (Orphanet:369)
Glycogen storage disease due to phosphorylase kinase deficiency (Orphanet:370)
Hereditary orotic aciduria (Orphanet:30)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Multiple sulfatase deficiency (Orphanet:585)
Neutral lipid storage disease (Orphanet:165)
Pearson syndrome (Orphanet:699)
Porphyria cutanea tarda (Orphanet:101330)
Refsum disease (Orphanet:773)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Sialidosis type 1 (Orphanet:812)
Sweet syndrome (Orphanet:3243)
X-linked sideroblastic anemia (Orphanet:75563)