Human Phenotype Ontology 
Grandparent Node:
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Abnormal cerebral cortex morphology (HP:0002538)help
Parent Node:
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Cortical dysplasia (HP:0002539)help
..Starting node
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Frontoparietal cortical dysplasia (HP:0006930)help
Term ID: 6930
Name: Frontoparietal cortical dysplasia
Synonym:
Definition: The presence of developmental dysplasia of the cortex of frontal lobe and the cortex of parietal lobe.
Comments:
Reference: HP:0006930
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006930HP:0006930Frontoparietal cortical dysplasia0TUBB2B CL E G H34773330829OMIM:610031Cortical dysplasia, complex, with other brain malformations 7.39


Genes (1) :TUBB2B

Diseases (1) :OMIM:610031
 

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