Human Phenotype Ontology 
Grandparent Node:
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Morphological central nervous system abnormality (HP:0002011)help
Parent Node:
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Abnormal meningeal morphology (HP:0010651)help
..Starting node
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Abnormal pia mater (HP:0100701)help
Term ID: 100701
Name: Abnormal pia mater
Synonym: Abnormality of the pia mater
Definition: An abnormality of the pia mater.
Comments:
Reference: HP:0100701
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal arachnoid mater morphology (HP:0100700) help
..expandAbnormal dura mater morphology (HP:0010652) help
..expandAbnormal spinal meningeal morphology (HP:0010303) help
..expandMeningeal calcification (HP:0100250) help
..expandMeningocele (HP:0002435) 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:0100701HP:0100701Abnormal pia mater0 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 December 15 2022 release.