Hypoammonemia

Symptom Information:

Symptom ID: HPO:0100493
Synonyms:
Hyperammonemia (disorder) [Orphanet:49120]
Hyperammonemia [Orphanet:49120]
Hypoammonemia [Orphanet:49120]
Hyperammonaemia [Orphanet:49120]
Hyperammonaemia [MedDRA:10020575]
Hyperammonemia [MedDRA:10020575]
Quality:
Cross references:
Orphanet:49120 "Hypoammonemia" [Orphanet:49120]
UMLS:C0220994 "Hyperammonemia" [Orphanet:49120]
Is a (Direct Parents):
MedDRA Protein metabolism disorders NEC
Orphanet Abnormality of metabolism/homeostasis
HPO         Abnormality of nitrogen compound homeostasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of nitrogen compound homeostasis(HPO:0004364)
             Hypoammonemia(HPO:0100493)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Protein and amino acid metabolism disorders NEC(MedDRA:10037008)
       Protein metabolism disorders NEC(MedDRA:10037009)
          Hypoammonemia(HPO:0100493)
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Oculocerebrorenal syndrome (Orphanet:534)