Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cerebral morphology (HP:0002060)help
Grandparent Node:
expandEctopic calcification (HP:0010766)help
Parent Node:
expandAbnormal cerebral white matter morphology (HP:0002500)help
Parent Node:
expandCerebral calcification (HP:0002514)help
..Starting node
..expandSubcortical white matter calcifications (HP:0007346)help
Term ID: 7346
Name: Subcortical white matter calcifications
Synonym:
Definition:
Comments:
Reference: HP:0007346
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasal ganglia calcification (HP:0002135) help
..expandBilateral intracerebral calcifications (HP:0005671) help
..expandCalcification of falx cerebri (HP:0005462) help
..expandChoroid plexus calcification (HP:0006960) help
..expandCongenital intracerebral calcification (HP:0006906) help
..expandDiffuse cerebral calcification (HP:0005849) help
..expandIntracerebral periventricular calcifications (HP:0007229) help
..expandMeningeal calcification (HP:0100250) help
..expandMidline brain calcifications (HP:0007045) help
..expandNonarteriosclerotic cerebral calcification (HP:0007238) help
..expandPituitary calcification (HP:0010513) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007346HP:0007346Subcortical white matter calcifications0ERCC6 CL E G H2074133540Cockayne syndrome B133540C0751038OMIM116453438609413
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :ERCC6

Diseases (1) :133540
 

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