Trait

Cerebral degeneration

Also called: Neuroaxonal degeneration in the brain
Body system: Abnormality of the nervous system

This page as data

Add .json to the page's address, or ask for application/json, to read it as JSON.

library(jsonlite)

url <- "https://dantelabs.com/traits/cerebral-degeneration.json"
page <- fromJSON(url)
page$trait$name

Open the JSON

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2 genes linked to Cerebral degeneration

Changes in these genes cause rare conditions in which Cerebral degeneration 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
GLB1galactosidase beta 1	Not recorded	In 1 condition
PANK2pantothenate kinase 2	Not recorded	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.

Broader traits

Atrophy/Degeneration affecting the cerebrum

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 2026.10.17-8666dff2.

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