Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
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Nervous System Diseases (D009422)
Parent Node:
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Signs and Symptoms (D012816)
..Starting node
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Neurologic Manifestations (D009461)

       Child Nodes:
........expandCerebrospinal Fluid Leak (D065634) Child2
........expandDecerebrate State (D003655)
........expandDiabetes Mellitus, Permanent Neonatal, With Neurologic Features (C563424)
........expandDyskinesias (D020820) Child199
........expandGait Disorders, Neurologic (D020233) Child2
........expandMeningism (D008580)
........expandNeurobehavioral Manifestations (D019954) Child701
........expandNeurogenic Inflammation (D020078)
........expandNeuromuscular Manifestations (D020879) Child103
........expandOrthostatic Intolerance (D054971) Child8
........expandPain (D010146) Child55
........expandParalysis (D010243) Child83
........expandParesis (D010291) Child10
........expandPsychophysiologic Disorders (D011602)
........expandPupil Disorders (D011681) Child20
........expandReflex, Abnormal (D012021) Child5
........expandSeizures (D012640) Child40
........expandSensation Disorders (D012678) Child478
........expandSleep Disorders (D012893) Child41
........expandSusac Syndrome (D055955)
........expandUrinary Bladder, Neurogenic (D001750)
........expandVertigo (D014717) Child5
........expandVoice Disorders (D014832) Child7



 Sister Nodes: 
..expandAging, Premature (D019588) Child1
..expandAsthenia (D001247)
..expandBody Temperature Changes (D001832) Child10
..expandBody Weight (D001835) Child59
..expandCardiac Output, High (D016534)
..expandCardiac Output, Low (D002303)
..expandChills (D023341)
..expandCyanosis (D003490) Child3
..expandEdema (D004487) Child11
..expandEye Manifestations (D005132) Child9
..expandFailure to Thrive (D005183) Child5
..expandFatigue (D005221) Child2
..expandFeminization (D005262)
..expandFetal Distress (D005316)
..expandFlushing (D005483) Child2
..expandHeart Murmurs (D006337) Child1
..expandHot Flashes (D019584)
..expandHypergammaglobulinemia (D006942) Child6
..expandHyperlactatemia (D065906)
..expandHypertriglyceridemic Waist (D064250)
..expandIntermittent Claudication (D007383)
..expandMobility Limitation (D051346)
..expandMotion Sickness (D009041) Child2
..expandNeurologic Manifestations (D009461) Child1586
..expandOral Manifestations (D009912) Child3
..expandPain (D010146) Child55
..expandPolydipsia (D059606) Child1
..expandProdromal Symptoms (D062706)
..expandPseudophakia (D019591)
..expandReticulocytosis (D045262)
..expandSigns and Symptoms, Digestive (D012817) Child50
..expandSigns and Symptoms, Respiratory (D012818) Child37
..expandSkin Manifestations (D012877) Child42
..expandUrological Manifestations (D020924) Child26
..expandVirilism (D014770) Child8
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7973
Name:Neurologic Manifestations
Definition:Clinical signs and symptoms caused by nervous system injury or dysfunction.
Alternative IDs:
ParentIDs:MESH:D009422|MESH:D012816
TreeNumbers:C10.597 |C23.888.592
Synonyms:Deficit, Focal Neurologic |Deficit, Neurologic |Deficits, Focal Neurologic |Deficits, Neurologic |Dysfunction, Neurologic |Dysfunctions, Neurologic |Finding, Neurologic |Findings, Neurologic |Focal Neurologic Deficit |Focal Neurologic Deficits |Manifestation, Neur
Slim Mappings:Nervous system disease|Signs and symptoms
Reference: MedGen: D009461
MeSH: D009461
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants