Hypoketotic hypoglycemia

Symptom Information:

Symptom ID: HPO:0001985
Synonyms:
Hypoglycemia, hypoketotic [HPO:0001985]
Hypoglycemia, hypoketotic [OMIM:Hypoglycemia, hypoketotic]
Hypoketotic hypoglycemia [OMIM:Hypoketotic hypoglycemia]
Hypoketotic hypoglycemia (in some patients) [OMIM:Hypoketotic hypoglycemia (in some patients)]
Quality:
Cross references:
OMIM: "Hypoglycemia, hypoketotic" [OMIM:Hypoglycemia, hypoketotic]
OMIM: "Hypoketotic hypoglycemia" [OMIM:Hypoketotic hypoglycemia]
OMIM: "Hypoketotic hypoglycemia (in some patients)" [OMIM:Hypoketotic hypoglycemia (in some patients)]
Is a (Direct Parents):
HPO         Hypoglycemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormal glucose homeostasis(HPO:0011014)
                Abnormality of blood glucose concentration(HPO:0011015)
                   Hypoglycemia(HPO:0001943)
                      Hypoketotic hypoglycemia(HPO:0001985)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:231530)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine palmitoyl transferase II deficiency, severe infantile form (Orphanet:228305)
Carnitine uptake deficiency (Orphanet:158)
Carnitine-acylcarnitine translocase deficiency (Orphanet:159)
DK1-CDG (Orphanet:91131)
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (Orphanet:71212)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)