Medical Subject Headings

Last uploaded: January 31, 2024
Preferred Name

Hereditary Sensory and Motor Neuropathy

Synonyms

Dejerine Sottas Disease

CMT4f

Definitions

A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)

ID

http://purl.bioontology.org/ontology/MESH/D015417

altLabel

Dejerine Sottas Disease

Hereditary, Type VII, Motor and Sensory Neuropathy

Dejerine Sottas Neuropathy

HMSN Type VIIs

Syndrome, Dejerine-Sottas

Hereditary Motor and Sensory Neuropathy

Dejerine-Sottas Syndrome

Dejerine-Sottas Neuropathy

Hereditary Motor and Sensory Neuropathy 3

HMSN Type IIIs

HMSN Type VII

Hereditary Motor and Sensory Neuropathies

Dejerine-Sottas Disease

Neuropathy, Dejerine-Sottas

Type VII, HMSN

Charcot-Marie-Tooth Disease, Type 3

Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

HMSN Type III

Dejerine-Sottas Hypertrophic Neuropathy

Hereditary Motor and Sensory Neuropathy Type III

HMSN3

HMSN

Hypertrophic Neuropathy of Dejerine Sottas

Hypertrophic Neuropathy of Dejerine-Sottas

Dejerine Sottas Syndrome

Hereditary, Type III, Motor and Sensory Neuropathy

Disease, Dejerine-Sottas

Charcot Marie Tooth Disease, Type 3

Herditary Sensory and Motor Neuropathy

Neuropathies, Hereditary Motor and Sensory

CMT4f

AN

do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES

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

C0027888

C0011195

C0019816

DC

1

definition

A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)

DX

19880101

HN

2000(1989)

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

Machine permutation

2000; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1988-1999

Mapped from

http://purl.bioontology.org/ontology/MESH/C563517

http://purl.bioontology.org/ontology/MESH/C536965

http://purl.bioontology.org/ontology/MESH/C564269

http://purl.bioontology.org/ontology/MESH/C563702

http://purl.bioontology.org/ontology/MESH/C564655

http://purl.bioontology.org/ontology/MESH/C565492

http://purl.bioontology.org/ontology/MESH/C562851

http://purl.bioontology.org/ontology/MESH/C536546

http://purl.bioontology.org/ontology/MESH/C564947

http://purl.bioontology.org/ontology/MESH/C564948

http://purl.bioontology.org/ontology/MESH/C537626

http://purl.bioontology.org/ontology/MESH/C566575

http://purl.bioontology.org/ontology/MESH/C537583

http://purl.bioontology.org/ontology/MESH/C535813

http://purl.bioontology.org/ontology/MESH/C535717

http://purl.bioontology.org/ontology/MESH/C563562

http://purl.bioontology.org/ontology/MESH/C565773

http://purl.bioontology.org/ontology/MESH/C536896

MDA

19991108

MMR

20180630

MN

C10.574.500.495

C10.668.829.800.300

C10.500.300

C16.131.666.300

C16.320.400.375

notation

D015417

prefLabel

Hereditary Sensory and Motor Neuropathy

TERMUI

T755169

T745673

T045523

T371177

T817093

T769515

T045522

T811481

T045519

T371167

T811486

T817092

T045518

T045524

T811480

T817094

T045521

T817089

T750855

T811482

TH

OMIM (2013)

NLM (2000)

UNK (19XX)

NLM (2013)

NLM (2010)

NLM (1988)

NLM (2011)

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

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/145900 OMIM CUI
http://purl.bioontology.org/ontology/SCTSPA/128204009 SCTSPA CUI
http://purl.bioontology.org/ontology/ICD10/G60.0 ICD10 CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027888 MEDLINEPLUS CUI
http://purl.bioontology.org/ontology/MDRFRE/10075469 MDRFRE CUI
http://purl.bioontology.org/ontology/NDFRT/N0000003229 NDFRT CUI
http://purl.bioontology.org/ontology/MDRGER/10075469 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10077306 MDRGER CUI
http://purl.bioontology.org/ontology/CSP/2042-7637 CRISP CUI
http://purl.bioontology.org/ontology/MEDDRA/10077306 MEDDRA CUI
http://purl.bioontology.org/ontology/RCD/F3610 RCD CUI
http://purl.bioontology.org/ontology/MEDDRA/10075469 MEDDRA CUI
http://purl.bioontology.org/ontology/ICD10CM/G60.0 ICD10CM CUI
http://purl.bioontology.org/ontology/SNMI/DA-44020 SNMI CUI
http://purl.bioontology.org/ontology/MSHFRE/D015417 MSHFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/398100001 SCTSPA CUI
http://purl.bioontology.org/ontology/SNOMEDCT/398100001 SNOMEDCT CUI
http://purl.bioontology.org/ontology/MDRFRE/10077306 MDRFRE CUI
http://purl.bioontology.org/ontology/SNMI/DA-44010 SNMI CUI
http://purl.bioontology.org/ontology/SCTSPA/111499002 SCTSPA CUI
http://purl.bioontology.org/ontology/RCD/F3600 RCD CUI
http://purl.bioontology.org/ontology/CSP/2042-7637 CRISP CUI
http://purl.bioontology.org/ontology/OMIM/304040 OMIM CUI
http://purl.bioontology.org/ontology/SNOMEDCT/111499002 SNOMEDCT CUI
http://purl.bioontology.org/ontology/ICD10CM/G60.0 ICD10CM CUI
http://purl.bioontology.org/ontology/MSHFRE/D015417 MSHFRE CUI
http://purl.bioontology.org/ontology/RCD/X00AD RCD CUI
http://purl.bioontology.org/ontology/MSHFRE/D015417 MSHFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/128204009 SNOMEDCT CUI
http://purl.jp/bio/4/id/200906092002132760 IOBC LOOM
http://purl.obolibrary.org/obo/OMIT_0016178 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.666.300 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D015417 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.400.375 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.829.800.300 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.500.495 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.500.300 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038417 PMAPP-PMO LOOM