Increased hepatic glycogen content
Symptom Information:
Symptom ID: | HPO:0006568 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |