Ketosis

Symptom Information:

Symptom ID: HPO:0001946
Synonyms:
Ketonemia [HPO:0001946]
Ketonaemia [HPO:0001946]
Ketonemia [OMIM:Ketonemia]
Ketosis [OMIM:Ketosis]
Ketosis [MedDRA:10023391]
Quality:
Cross references:
OMIM: "Ketonemia" [OMIM:Ketonemia]
OMIM: "Ketosis" [OMIM:Ketosis]
UMLS:C0022638 "Ketosis" [HPO:0001946]
UMLS:C0235430 "Ketonaemia" [HPO:0001946]
Is a (Direct Parents):
MedDRA Metabolic acidoses (excl diabetic acidoses)
HPO         Abnormality of metabolism/homeostasis
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)
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)