Medical Subject Headings

Last uploaded: January 31, 2024
Preferred Name

Hereditary Sensory and Autonomic Neuropathies

Synonyms

Sensory Neuropathies, Congenital

Hereditary Sensory Neuropathy

Definitions

A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)

ID

http://purl.bioontology.org/ontology/MESH/D009477

altLabel

Sensory Neuropathies, Congenital

Neuropathy, Congenital Sensory, with Anhidrosis

Sensory Neuropathies, Hereditary

Hereditary Sensory and Autonomic Neuropathy Type I

Sensory and Autonomic Neuropathies, Hereditary

Giaccai Type Acroosteolysis

Hereditary Sensory and Autonomic Neuropathy, Type 4

Hereditary Sensory Autonomic Neuropathy, Type 4

Hereditary Sensory Radicular Neuropathy

Hereditary Sensory Radicular Neuropathy, Recessive Form

Neuropathy, Congenital Sensory

Congenital Insensitivity to Pain with Anhidrosis

Neuropathy Hereditary Sensory Radicular, Autosomal Dominant

Sensory Neuropathy, Hereditary

HSAN2

Hereditary Sensory Neuropathy Type Ia

Neuropathy, Hereditary Sensory, Type I

HSAN 5

Acroosteolysis, Giaccai Type

HSAN Type V

Neuropathies, Hereditary Sensory and Autonomic

Hereditary Sensory Neuropathy Type 1

Type I, HSAN

Familial Dysautonomia, Type II

Hereditary Sensory and Autonomic Neuropathy Type 2

Hereditary Sensory and Autonomic Neuropathy Type IV

Acroosteolyses, Neurogenic

Neuropathy, Hereditary Sensory And Autonomic, Type V

HSAN 4

Hereditary Sensory And Autonomic Neuropathy IV

HSANs (Hereditary Sensory Autonomic Neuropathy)

Hereditary Sensory Neuropathies

Congenital Sensory Neuropathy

HSAN Type I

Hereditary Sensory and Autonomic Neuropathy Type V

Neuropathies, Hereditary Sensory

Neurogenic Acroosteolysis

Hereditary Sensory and Autonomic Neuropathy, Type 5

Hereditary Sensory and Autonomic Neuropathy Type II

Neuropathy, Hereditary Sensory And Autonomic, Type I

HSN Type I

HSAN 1

HSN Type IIs

Congenital Sensory Neuropathies

Neuropathy, Hereditary Sensory

Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant

HSAN

Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive

HSAN Type II

HSAN Type IV

Neuropathy Hereditary Sensory and Autonomic Type 1

Pain Insensitivity with Anhidrosis, Congenital

Hereditary Sensory Autonomic Neuropathy, Type 1

Neuropathy, Progressive Sensory, Of Children

HSAN (Hereditary Sensory Autonomic Neuropathy)

Type IV, HSAN

Hereditary Sensory and Autonomic Neuropathy Type 1

HSAN IV

HSAN V

HSN Type II

Neuropathies, Congenital Sensory

Familial Dysautonomia, Type 2

Insensitivity to Pain with Anhidrosis, Congenital

Hereditary Sensory and Autonomic Neuropathy 4

HSAN I

Acroosteolysis, Neurogenic

Neurogenic Acroosteolyses

Sensory Neuropathy, Congenital

Hereditary Sensory Autonomic Neuropathy, Type 5

HSAN5

Type I, HSN

Hereditary Sensory Autonomic Neuropathy, Type 2

HSANII

Hereditary Sensory Neuropathy Type I

Insensitivity to Pain, Congenital, with Anhidrosis

Hereditary Sensory Neuropathy

AN

do not confuse with HEREDITARY SENSORY AND MOTOR NEUROPATHY; note entry terms for HSAN types: HSAN TYPE III see DYSAUTONOMIA, FAMILIAL is also available

AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0699739

C0020074

C0086405

C0020072

C0027889

C0020075

C0020071

DC

1

definition

A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)

DX

19790101

FX

D000699

HN

2000(1989); use NEUROPATHY, HEREDITARY SENSORY 1979-1988

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000469

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D000699

Machine permutation

2000; see NEUROPATHIES, HEREDITARY SENSORY AND AUTONOMIC 1989-1999; see NEUROPATHY, HEREDITARY SENSORY 1979-1988

Mapped from

http://purl.bioontology.org/ontology/MESH/C580162

http://purl.bioontology.org/ontology/MESH/C564296

http://purl.bioontology.org/ontology/MESH/C567738

http://purl.bioontology.org/ontology/MESH/C563870

http://purl.bioontology.org/ontology/MESH/C535624

http://purl.bioontology.org/ontology/MESH/C564090

http://purl.bioontology.org/ontology/MESH/C537956

MDA

19991108

MMR

20180630

MN

C10.500.250

C16.320.400.415

C16.131.666.310

C10.668.829.800.175

C10.574.500.493

notation

D009477

prefLabel

Hereditary Sensory and Autonomic Neuropathies

TERMUI

T028245

T755149

T818696

T843028

T028244

T824571

T751022

T365291

T365287

T028251

T811628

T751016

T028246

T843031

T028254

T818698

T843029

T841185

T751012

T028252

T841655

T818699

T751017

T751021

T028249

T365290

T751023

T841652

T841654

T028247

T028253

T751024

T811629

T841653

T751014

T843887

T751018

T824572

T365289

T751015

T811624

T028250

T028248

T811626

T811625

T751011

T365288

T751019

T811636

T365286

T843030

T812405

T365295

T818697

T751013

T841649

T811627

T365292

T028255

T841650

TH

NLM (1979)

OMIM (2013)

NLM (2000)

UNK (19XX)

NLM (2010)

GHR (2014)

NLM (2014)

ORD (2010)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D009421

http://purl.bioontology.org/ontology/MESH/D011115

http://purl.bioontology.org/ontology/MESH/D020271

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MDRFRE/10040037 MDRFRE CUI
http://purl.bioontology.org/ontology/RCD/X00AJ RCD CUI
http://purl.bioontology.org/ontology/MSHFRE/D009477 MSHFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/128205005 SCTSPA CUI
http://purl.bioontology.org/ontology/SCTSPA/128206006 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/162400 OMIM CUI
http://purl.bioontology.org/ontology/SCTSPA/11442006 SCTSPA CUI
http://purl.bioontology.org/ontology/ICD9CM/356.2 ICD9CM CUI
http://purl.bioontology.org/ontology/CSP/2042-6678 CRISP CUI
http://purl.bioontology.org/ontology/MDRGER/10040037 MDRGER CUI
http://purl.bioontology.org/ontology/SNOMEDCT/11442006 SNOMEDCT CUI
http://purl.bioontology.org/ontology/MSHFRE/D009477 MSHFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10019901 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRGER/10019901 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10040037 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10019901 MDRFRE CUI
http://purl.bioontology.org/ontology/SNMI/DA-44030 SNMI CUI
http://purl.bioontology.org/ontology/SCTSPA/62985007 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/256800 OMIM CUI
http://purl.bioontology.org/ontology/SNMI/DA-44034 SNMI CUI
http://purl.bioontology.org/ontology/MSHFRE/D009477 MSHFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/62985007 SNOMEDCT CUI
http://purl.bioontology.org/ontology/OMIM/191315 OMIM CUI
http://purl.bioontology.org/ontology/SNOMEDCT/128205005 SNOMEDCT CUI
http://purl.bioontology.org/ontology/RCD/X00AF RCD CUI
http://purl.bioontology.org/ontology/MSHFRE/D009477 MSHFRE CUI
http://purl.bioontology.org/ontology/NDFRT/N0000002179 NDFRT CUI
http://purl.bioontology.org/ontology/SNOMEDCT/128206006 SNOMEDCT CUI
http://purl.bioontology.org/ontology/OMIM/162030 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/608654 OMIM CUI
http://purl.bioontology.org/ontology/RCD/X00AK RCD CUI
http://purl.bioontology.org/ontology/SNOMEDCT/230553002 SNOMEDCT CUI
http://purl.bioontology.org/ontology/SNOMEDCT/397734008 SNOMEDCT CUI
http://purl.bioontology.org/ontology/SNMI/DA-44031 SNMI CUI
http://purl.bioontology.org/ontology/RCD/X00AG RCD CUI
http://purl.bioontology.org/ontology/SCTSPA/397734008 SCTSPA CUI
http://purl.bioontology.org/ontology/SCTSPA/230553002 SCTSPA CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.666.310 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0010503 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.114.750.137 RH-MESH LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12556 BIRNLEX LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12556 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12556 NIFSTD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D009477 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.500.310 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.400.415 RH-MESH LOOM
http://purl.jp/bio/4/id/200906009601258025 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C20.111.258.750.600 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038416 PMAPP-PMO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.314.750.600 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.829.800.750.450 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.500.496 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.829.800.625 RH-MESH LOOM