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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Abnormal meningeal morphology (HP:0010651)help
Parent Node:
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Cerebral calcification (HP:0002514)help
..Starting node
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Meningeal calcification (HP:0100250)help
Term ID: 100250
Name: Meningeal calcification
Synonym:
Definition: Calcium deposition affecting the Meninges.
Comments:
Reference: HP:0100250
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
..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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100250HP:0100250Meningeal calcification0COL11A1 CL E G H13012186OMIM:154780Marshall syndrome.215


Genes (1) :COL11A1

Diseases (1) :OMIM:154780
 

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