Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal cerebral morphology (HP:0002060)help
Grandparent Node:
expand
Ectopic calcification (HP:0010766)help
Parent Node:
expand
Cerebral calcification (HP:0002514)help
..Starting node
..expand
Bilateral intracerebral calcifications (HP:0005671)help
Term ID: 5671
Name: Bilateral intracerebral calcifications
Synonym: Bilateral intracranial calcifications
Definition: Deposition of calcium salts on both sides of the brain.
Comments:
Reference: HP:0005671
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasal ganglia calcification (HP:0002135) 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
..expandSubcortical white matter calcifications (HP:0007346) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0005671HP:0005671Bilateral intracerebral calcifications0ECM1 CL E G H1893247100Lipid proteinosis247100C0023795OMIM11063153602201
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :ECM1

Diseases (1) :247100
 

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