Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal nervous system physiology (HP:0012638)help
Parent Node:
expand
Encephalopathy (HP:0001298)help
..Starting node
..expand
Infantile encephalopathy (HP:0007105)help
Term ID: 7105
Name: Infantile encephalopathy
Synonym:
Definition: Encephalopathy with onset in the infantile period.
Comments:
Reference: HP:0007105
Genes and Diseases:
 
       Child Nodes:

 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
..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


Genes (8) :CCDC88A D2HGDH GCDH SLC19A3 STXBP1 TK2 TSEN54 ZNHIT3

Diseases (8) :OMIM:617507 OMIM:600721 OMIM:231670 ORPHA:263410 OMIM:612164 ORPHA:254875 OMIM:225753 OMIM:260565
 

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