Human Phenotype Ontology 
..Starting node
..expandHypophenylalaninemia (HP:0500141)help
Term ID: 500141
Name: Hypophenylalaninemia
Synonym: Decreased blood phenylalanine; Low blood phenylalanine
Definition: A decreased amount of phenylalanine in the blood.
Comments:
Reference: HP:0500141
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500141HP:0500141Hypophenylalaninemia0 CL E G H


Genes (0) :

Diseases (0) :
 

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