Ketosis
Symptom Information:
Symptom ID: | HPO:0001946 | |||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Ketosis(HPO:0001946) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Acid-base disorders(MedDRA:10000485) Metabolic acidoses (excl diabetic acidoses)(MedDRA:10027416) Ketosis(HPO:0001946) |
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Database Frequency: | 17 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Classic maple syrup urine disease | (Orphanet:268145) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Fructose-1,6-bisphosphatase deficiency | (Orphanet:348) |
GLYCOGEN STORAGE DISEASE IXc | (OMIM:613027) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Glycogen storage disease due to hepatic glycogen synthase deficiency | (Orphanet:2089) |
Glycogen storage disease due to liver phosphorylase kinase deficiency | (Orphanet:264580) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Malonic aciduria | (Orphanet:943) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
TIGLIC ACIDEMIA | (OMIM:275190) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |