Warning: The NCBI web site requires JavaScript to function. more...

MedGen

National Center for Biotechnology Information

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

Neuropathy, hereditary sensory and autonomic, type IA, severe

MedGen UID:: 1695379
•Concept ID:: C5231533
•: Disease or Syndrome

Synonym:	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA, SEVERE

OMIM®:	605712

Supplemental Content

Table of contents

Clinical resources

ClinicalTrials.gov

Practice guidelines

Bookshelf
See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

Consumer resources

MedlinePlus

Reviews

Related information

ClinVar
Related medical variations
OMIM
Related records in OMIM
PubMed (OMIM)
Related literature resources in PubMed

Recent activity

Clear Turn Off Turn On

Neuropathy, hereditary sensory and autonomic, type IA, severe
Neuropathy, hereditary sensory and autonomic, type IA, severe

MedGen
C5231533[conceptid] (1)
MedGen
C2751092[trait identifier] AND "OMIM"[submitter] (5)
ClinVar
C3150896[trait identifier] AND "OMIM"[submitter] (5)
ClinVar
C2752089[trait identifier] AND "OMIM"[submitter] (27)
ClinVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...