Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
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Preferred Name

Nystagmus, Congenital
Synonyms

Congenital Nystagmus
Definitions

Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with ALBINISM and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)
ID

http://purl.bioontology.org/ontology/MESH/D020417
altLabel

Congenital Nystagmus
AN

do not use /congen; do not coord with INFANT, NEWBORN, DISEASES
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

C0700501
DC

1
definition

Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with ALBINISM and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)
DX

20000101
HN

2000
Inverse of AQ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

2000
Mapped from

http://purl.bioontology.org/ontology/MESH/C580539

http://purl.bioontology.org/ontology/MESH/C537444

http://purl.bioontology.org/ontology/MESH/C564938

http://purl.bioontology.org/ontology/MESH/C537159

http://purl.bioontology.org/ontology/MESH/C563394

http://purl.bioontology.org/ontology/MESH/C537855

http://purl.bioontology.org/ontology/MESH/C537854

http://purl.bioontology.org/ontology/MESH/C566292

http://purl.bioontology.org/ontology/MESH/C564478

http://purl.bioontology.org/ontology/MESH/C566192

http://purl.bioontology.org/ontology/MESH/C537858

http://purl.bioontology.org/ontology/MESH/C565876

http://purl.bioontology.org/ontology/MESH/C565005

http://purl.bioontology.org/ontology/MESH/C537853

http://purl.bioontology.org/ontology/MESH/C537856
MDA

19991108
MN

C11.590.400.300

C10.292.562.675.300

C16.614.643
notation

D020417
prefLabel

Nystagmus, Congenital
TERMUI

T358317

T370617
TH

NLM (2000)
tui

T019
subClassOf

http://purl.bioontology.org/ontology/MESH/D009759

http://purl.bioontology.org/ontology/MESH/D007232
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU034700 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU034700 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU053438 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/H55.01 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI