Trait

Neuropathic arthropathy

Also called: Charcot arthropathy, Charcot joint
Body system: Abnormality of the musculoskeletal system

This page as data

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library(jsonlite)

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

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6 genes linked to Neuropathic arthropathy

Changes in these genes cause rare conditions in which Neuropathic arthropathy 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
ATL3atlastin GTPase 3	Often (30–79%)	In 2 conditions
NTRK1neurotrophic receptor tyrosine kinase 1	Often (30–79%)	In 2 conditions
ATL1atlastin GTPase 1	Sometimes (5–29%)	In 1 condition
SPTLC1serine palmitoyltransferase long chain base subunit 1	Sometimes (5–29%)	In 1 condition
SPTLC2serine palmitoyltransferase long chain base subunit 2	Sometimes (5–29%)	In 1 condition
ELP1elongator acetyltransferase complex subunit 1	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

Disease of the joints

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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