Human Phenotype Ontology 
Grandparent Node:
expandAbnormal nervous system physiology (HP:0012638)help
Parent Node:
expandEncephalopathy (HP:0001298)help
..Starting node
..expandCongenital encephalopathy (HP:0007239)help
Term ID: 7239
Name: Congenital encephalopathy
Synonym:
Definition:
Comments:
Reference: HP:0007239
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute encephalopathy (HP:0006846) 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
..expandNonprogressive encephalopathy (HP:0007030) help
..expandProgressive encephalopathy (HP:0002448) help
..expandRecurrent encephalopathy (HP:0007335) 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:0007239HP:0007239Congenital encephalopathy0 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.