Human Phenotype Ontology 
Grandparent Node:
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Abnormality of metabolism/homeostasis (HP:0001939)help
Parent Node:
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Abnormal circulating nitrogen compound concentration (HP:0004364)help
..Starting node
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Hypoammonemia (HP:0100493)help
Term ID: 100493
Name: Hypoammonemia
Synonym:
Definition: A decreased concentration of ammonia in the blood.
Comments:
Reference: HP:0100493
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal circulating biopterin concentration (HP:0040210) help
..expandAbnormal circulating creatinine concentration (HP:0012100) help
..expandAbnormal circulating neopterin concentration (HP:0040206) help
..expandAzotemia (HP:0002157) help
..expandEpisodic ammonia intoxication (HP:0001951) help
..expandHyperuricosuria (HP:0003149) help
..expandIncreased level of allantoin in serum (HP:0410052) help
..expandUrocanic aciduria (HP:0012237) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100493HP:0100493Hypoammonemia0OCRL CL E G H49528108ORPHA:534Oculocerebrorenal syndrome of LoweHP:0040283 - Occasional88


Genes (1) :OCRL

Diseases (1) :ORPHA:534
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.