NGF and Hereditary Sensory And Autonomic Neuropathy: Association Evidence

Gene-Disorder Association · Article

Gene

NGF

Nerve Growth Factor

Disorder

Hereditary Sensory And Autonomic Neuropathy

First reported 2000

Supporting publications 1

Key publication · gene–disorder The Gly571Arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor.Journal of cellular physiology · 2000

Key publication · disorder Progressive muscular atrophy of the peroneal type (Charcot-Marie-Tooth disease) orthopaedic management and end-result study.The Journal of bone and joint surgery. American volume · 1950

Manually curated

Association Review

In brief

The association between NGF (Nerve Growth Factor) and Hereditary Sensory And Autonomic Neuropathy is reported, with clinical genetic testing available.

Sources 1

Clinical variants 0

Symptoms 0

Compounds 0

Trials 0

Publications 1

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access

Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access

NGF

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

Request access

Hereditary Sensory And Autonomic Neuropathy

The disorder

9 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access

Literature

Reading

1 publication

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Request access

Provenance

References & sources

4 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access