Human Phenotype Ontology 
Grandparent Node:
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Abnormal cerebral morphology (HP:0002060)help
Grandparent Node:
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Ectopic calcification (HP:0010766)help
Parent Node:
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Cerebral calcification (HP:0002514)help
..Starting node
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Congenital intracerebral calcification (HP:0006906)help
Term ID: 6906
Name: Congenital intracerebral calcification
Synonym:
Definition: The presence of calcium deposition within brain structures that is present already at the time of birth.
Comments:
Reference: HP:0006906
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
..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:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006906HP:0006906Congenital intracerebral calcification0 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 August 2021 release.