Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Encephalopathy (HP:0001298)help
..Starting node
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Nonprogressive encephalopathy (HP:0007030)help
Term ID: 7030
Name: Nonprogressive encephalopathy
Synonym:
Definition:
Comments:
Reference: HP:0007030
Genes and Diseases:
 
       Child Nodes:
........expandProfound static encephalopathy (HP:0007069) help

 Sister Nodes: 
..expandAcute encephalopathy (HP:0006846) help
..expandCongenital encephalopathy (HP:0007239) help
..expandEpileptic encephalopathy (HP:0200134) help
..expandHepatic encephalopathy (HP:0002480) help
..expandHypoglycemic encephalopathy (HP:0006929) help
..expandInfantile encephalopathy (HP:0007105) help
..expandMitochondrial encephalopathy (HP:0006789) help
..expandNecrotizing encephalopathy (HP:0006976) help
..expandProgressive encephalopathy (HP:0002448) help
..expandRecurrent encephalopathy (HP:0007335) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007030HP:0007030Nonprogressive encephalopathy0KYNU CL E G H8942236800Hydroxykynureninuria236800C0268474OMIM1816469605197
HP:0007030HP:0007069Profound static encephalopathy1KYNU CL E G H8942236800Hydroxykynureninuria236800C0268474OMIM1816469605197
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :KYNU UNC80

Diseases (2) :236800 616801
 

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