Human Phenotype Ontology 
Grandparent Node:
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Encephalopathy (HP:0001298)help
Parent Node:
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Acute encephalopathy (HP:0006846)help
..Starting node
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Acute necrotizing encephalopathy (HP:0006965)help
Term ID: 6965
Name: Acute necrotizing encephalopathy
Synonym:
Definition:
Comments:
Reference: HP:0006965
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006965HP:0006965Acute necrotizing encephalopathy0NDUFS4 CL E G H4724252010Mitochondrial complex I deficiency252010C1838979OMIM117977711602694
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :NDUFS4

Diseases (1) :252010
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.