Medical Subject Headings

Last uploaded: January 31, 2024
Preferred Name

Unverricht-Lundborg Syndrome

Synonyms

Disease, Unverricht-Lundborg

Definitions

An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, DYSARTHRIA, and intention tremor. Myoclonic seizures are severe and continuous, and tend to be triggered by movement, stress, and sensory stimuli. The age of onset is between 8 and 13 years, and the condition is relatively frequent in the Baltic region, especially Finland. (From Menkes, Textbook of Child Neurology, 5th ed, pp109-110)

ID

http://purl.bioontology.org/ontology/MESH/D020194

altLabel

Disease, Unverricht-Lundborg

Epilepsy, Progressive Myoclonic Type 1

Progressive Myoclonus Epilepsy 1

Myoclonus, Baltic

Epilepsies, Baltic Myoclonic

Epilepsy, Baltic Myoclonic

Syndrome, Unverricht-Lundborg

Myoclonic Epilepsy, Baltic

Myoclonus Epilepsies, Baltic

Myoclonus Epilepsy, Baltic

Myoclonic Epilepsy, Mediterranean

Unverricht Disease

Myoclonic Epilepsies, Baltic

Unverricht-Lundborg Disease

Epilepsy, Mediterranean Myoclonic

Unverricht Lundborg Disease

Lundborg Unverricht Syndrome

Progressive Myoclonus Epilepsybaltic Myoclonic Epilepsy

Unverricht Diseases

Epilepsy, Progressive Myoclonic 1

Baltic Myoclonic Epilepsy

Baltic Myoclonus

Diseases, Unverricht

Mediterranean Myoclonic Epilepsy

Myoclonus Progressive Epilepsy of Unverricht and Lundborg

Epilepsy, Baltic Myoclonus

Epilepsy, Progressive Myoclonic 1a

Baltic Myoclonus Epilepsy

Unverricht Lundborg Syndrome

Myoclonic Epilepsy of Unverricht and Lundborg

Baltic Myoclonus Epilepsies

Epilepsy, Progressive Myoclonus 1

Syndrome, Lundborg-Unverricht

Lundborg-Unverricht Syndrome

Diseases, Unverricht-Lundborg

Baltic Myoclonic Epilepsies

Epilepsies, Baltic Myoclonus

Unverricht-Lundborg Diseases

Disease, Unverricht

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

C0751785

DC

1

definition

An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, DYSARTHRIA, and intention tremor. Myoclonic seizures are severe and continuous, and tend to be triggered by movement, stress, and sensory stimuli. The age of onset is between 8 and 13 years, and the condition is relatively frequent in the Baltic region, especially Finland. (From Menkes, Textbook of Child Neurology, 5th ed, pp109-110)

DX

20000101

FX

D055313

HN

2000; for LUNDBORG-UNVERRICHT SYNDROME use EPILEPSY, MYOCLONIC 1977-1999

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/D055313

Machine permutation

2000; for LUNDBORG-UNVERRICHT SYNDROME see EPILEPSY, MYOCLONIC 1977-1999

MDA

19991103

MMR

20170224

MN

C10.228.140.490.375.130.650.900

C10.228.140.490.493.063.650.900

C16.320.400.940

C10.574.500.875

notation

D020194

prefLabel

Unverricht-Lundborg Syndrome

TERMUI

T781555

T014728

T370869

T358656

T781553

T812465

T370868

T812463

T781557

T812464

T370867

T781554

T842638

T370870

T781556

T842636

TH

OMIM (2013)

NLM (2000)

NLM (2012)

UNK (19XX)

GHR (2014)

ORD (2010)

tui

T047

subClassOf

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

http://purl.bioontology.org/ontology/MESH/D020191

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MSHFRE/D020194 MSHFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10054858 MDRGER CUI
http://purl.bioontology.org/ontology/MDRGER/10054894 MDRGER CUI
http://purl.bioontology.org/ontology/SNMI/DA-31590 SNMI CUI
http://purl.bioontology.org/ontology/OMIM/254800 OMIM CUI
http://purl.bioontology.org/ontology/MDRFRE/10054858 MDRFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/230423006 SNOMEDCT CUI
http://purl.bioontology.org/ontology/NDFRT/N0000004032 NDFRT CUI
http://purl.bioontology.org/ontology/MEDDRA/10054894 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRGER/10054895 MDRGER CUI
http://purl.bioontology.org/ontology/MDRFRE/10054894 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10054858 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10054895 MDRFRE CUI
http://purl.bioontology.org/ontology/OMIM/601145 OMIM CUI
http://purl.bioontology.org/ontology/RCD/X006V RCD CUI
http://purl.bioontology.org/ontology/SCTSPA/230423006 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDDRA/10054895 MEDDRA CUI
http://purl.bioontology.org/ontology/CSP/0485-7984 CRISP CUI
http://purl.obolibrary.org/obo/MONDO_0009698 EFO LOOM
http://purl.obolibrary.org/obo/DOID_3535 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0009698 MONDO LOOM
http://purl.obolibrary.org/obo/DOID_3535 BAO LOOM
http://purl.obolibrary.org/obo/DOID_3535 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_3535 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_3535 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_3535 FNS-H LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.500.875 RH-MESH LOOM
http://purl.obolibrary.org/obo/MONDO_0009698 DOVES LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/230423006 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/OMIT_0020110 OMIT LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12725 BIRNLEX LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12725 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12725 NIFSTD LOOM
http://purl.jp/bio/4/id/200906063627596055 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D020194 RH-MESH LOOM
http://id.nlm.nih.gov/mesh/D020194 MDM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.400.940 RH-MESH LOOM
http://purl.bioontology.org/ontology/RCD/X006V RCD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.490.250.650.900 RH-MESH LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_3535 NATPRO LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038245 PMAPP-PMO LOOM