Impaired gluconeogenesis

Symptom Information:

Symptom ID: HPO:0005959
Synonyms:
Gluconeogenesis impaired [HPO:0005959]
Impaired gluconeogenesis [OMIM:Impaired gluconeogenesis]
Quality:
Cross references:
OMIM: "Impaired gluconeogenesis" [OMIM:Impaired gluconeogenesis]
Is a (Direct Parents):
HPO         Abnormal glucose homeostasis
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)
                Impaired gluconeogenesis(HPO:0005959)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Carnitine uptake deficiency (Orphanet:158)
Phosphoenolpyruvate carboxykinase 1 deficiency (Orphanet:79316)
Phosphoenolpyruvate carboxykinase 2 deficiency (Orphanet:79317)
Phosphoenolpyruvate carboxykinase deficiency (Orphanet:2880)