Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cerebral subcortex morphology (HP:0010993)help
Parent Node:
expandAbnormal cerebral white matter morphology (HP:0002500)help
..Starting node
..expandWhite mater abnormalities in the posterior periventricular region (HP:0006812)help
Term ID: 6812
Name: White mater abnormalities in the posterior periventricular region
Synonym:
Definition:
Comments:
Reference: HP:0006812
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal corpus callosum morphology (HP:0001273) help
..expandAbnormal periventricular white matter morphology (HP:0002518) help
..expandAbnormality of the anterior commissure (HP:0030301) help
..expandAbnormality of the bed nucleus of stria terminalis (HP:0030798) help
..expandAbnormality of the internal capsule (HP:0012502) help
..expandAplasia/Hypoplasia of the cerebral white matter (HP:0012429) help
..expandCerebral white matter atrophy (HP:0012762) help
..expandDiffuse swelling of cerebral white matter (HP:0007341) help
..expandDiffuse white matter abnormalities (HP:0007204) help
..expandFocal white matter lesions (HP:0007042) help
..expandHyperintensity of cerebral white matter on MRI (HP:0030890) help
..expandHypointensity of cerebral white matter on MRI (HP:0007103) help
..expandMultifocal cerebral white matter abnormalities (HP:0007052) help
..expandSubcortical white matter calcifications (HP:0007346) 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:0006812HP:0006812White mater abnormalities in the posterior periventricular region0NAGA CL E G H46687631OMIM:609242Kanzaki disease.47


Genes (1) :NAGA

Diseases (1) :OMIM:609242
 

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