Human Phenotype Ontology 
Grandparent Node:
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Abnormality of digestive system physiology (HP:0025032)help
Parent Node:
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Abnormality of hepatobiliary system physiology (HP:0025155)help
..Starting node
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Decreased mitochondrial complex III activity in liver tissue (HP:0006558)help
Term ID: 6558
Name: Decreased mitochondrial complex III activity in liver tissue
Synonym:
Definition: Decreased activity of complex III of the mitochondrion in the liver.
Comments:
Reference: HP:0006558
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDecreased liver function (HP:0001410) help
..expandReye syndrome-like episodes (HP:0006582) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006558HP:0006558Decreased mitochondrial complex III activity in liver tissue0BCS1L CL E G H617124000Mitochondrial complex III deficiency124000C1852372OMIM14131020603647
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :BCS1L

Diseases (1) :124000
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.