Human Phenotype Ontology 
Grandparent Node:
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Abnormal cortical gyration (HP:0002536)help
Parent Node:
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Polymicrogyria (HP:0002126)help
..Starting node
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Frontal polymicrogyria (HP:0006821)help
Term ID: 6821
Name: Frontal polymicrogyria
Synonym: Polymicrogyria, anterior to posterior gradient
Definition: A type of polymicrogyria with a gradient of severity (anterior more severe than posterior) extending from frontal poles posteriorly to precentral gyrus and inferiorly to frontal operculum.
Comments:
Reference: HP:0006821
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandobsolete Frontoparietal polymicrogyria (HP:0007095) help
..expandPerisylvian polymicrogyria (HP:0012650) help
..expandUnilateral polymicrogyria (HP:0006927) 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:0006821HP:0006821Frontal polymicrogyria0ADGRG1 CL E G H92894512OMIM:606854Polymicrogyria, bilateral frontoparietal88
HP:0006821HP:0006821Frontal polymicrogyria0AHI1 CL E G H5480621575OMIM:608629Joubert syndrome 3175
HP:0006821HP:0006821Frontal polymicrogyria0DYNC1H1 CL E G H17782961OMIM:614563Mental retardation, autosomal dominant 13427
HP:0006821HP:0006821Frontal polymicrogyria0PPFIBP1 CL E G H84969249OMIM:620024
HP:0006821HP:0006821Frontal polymicrogyria0TUBB3 CL E G H1038120772OMIM:614039Cortical dysplasia, complex, with other brain malformations 164


Genes (5) :ADGRG1 AHI1 DYNC1H1 PPFIBP1 TUBB3

Diseases (5) :OMIM:606854 OMIM:608629 OMIM:614563 OMIM:620024 OMIM:614039
 

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