neuropathy, hereditary sensory, type 1F

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Disease Overview

Any hereditary sensory and autonomic neuropathy type 1 in which the cause of the disease is a mutation in the ATL3 gene.

Synonyms

ATL3 hereditary sensory and autonomic neuropathy type 1
HSN 1F
HSN1F
hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3
hereditary sensory neuropathy type 1F
hereditary sensory neuropathy type IF
neuropathy, hereditary sensory, type 1F
neuropathy, hereditary sensory, type IF

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.