Trait

Abnormal cerebral morphology

Any structural abnormality of the telencephalon, which is also known as the cerebrum.

HPO HP:0002060

Also called: Abnormality of the cerebrum, Abnormality of the telencephalon, Cerebral lesion
Body system: Abnormality of the nervous system

Reference genomeGRCh38hg38

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5 genes linked to Abnormal cerebral morphology

Changes in these genes cause rare conditions in which Abnormal cerebral morphology is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

Gene	How often it is seen	Conditions
ALG3ALG3 alpha-1,3- mannosyltransferase	Very often (80–99%)	In 1 condition
ZNF335zinc finger protein 335	Very often (80–99%)	In 1 condition
TOE1target of EGR1, exonuclease	Often (30–79%)	In 1 condition
JPH3junctophilin 3	Sometimes (5–29%)	In 1 condition
LRPPRCleucine rich pentatricopeptide repeat containing	Sometimes (5–29%)	In 1 condition

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Narrower traits

Broader traits

Abnormal shape of forebrain

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
Data release 2026.10.16-c6eea6bf.

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