Term ID: |
6930 |
Name: |
Frontoparietal cortical dysplasia |
Synonym: |
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Definition: |
The presence of developmental dysplasia of the cortex of frontal lobe and the cortex of parietal lobe. |
Comments: |
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Reference: |
HP:0006930 |
Genes and Diseases: | |
Child Nodes: |
Sister Nodes: |
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.
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