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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Neurologic Manifestations (D009461)
..Starting node ..Sensation Disorders (D012678)
Child Nodes:
........Dizziness (D004244) 1
........Hearing Disorders (D006311) 403
........Olfaction Disorders (D000857) 4
........Posterior column ataxia (C536342)
........Somatosensory Disorders (D020886) 6
........Taste Disorders (D013651) 3
........Vision Disorders (D014786) 84
Sister Nodes:
..Cerebrospinal Fluid Leak (D065634) 2
..Decerebrate State (D003655)
..Diabetes Mellitus, Permanent Neonatal, With Neurologic Features (C563424)
..Dyskinesias (D020820) 199
..Gait Disorders, Neurologic (D020233) 2
..Meningism (D008580)
..Neurobehavioral Manifestations (D019954) 701
..Neurogenic Inflammation (D020078)
..Neuromuscular Manifestations (D020879) 103
..Orthostatic Intolerance (D054971) 8
..Pain (D010146) 55
..Paralysis (D010243) 83
..Paresis (D010291) 10
..Psychophysiologic Disorders (D011602)
..Pupil Disorders (D011681) 20
..Reflex, Abnormal (D012021) 5
..Seizures (D012640) 40
..Sensation Disorders (D012678) 478
..Sleep Disorders (D012893) 41
..Susac Syndrome (D055955)
..Urinary Bladder, Neurogenic (D001750)
..Vertigo (D014717) 5
..Voice Disorders (D014832) 7
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10124
Name:	Sensation Disorders
Definition:	Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM).
Alternative IDs:
ParentIDs:	MESH:D009461
TreeNumbers:	C10.597.751 \|C23.888.592.763
Synonyms:	Sensation Disorder \|Senses Disorder, Special \|Senses Disorders, Special \|Sensory Disorder \|Sensory Disorders \|Special Senses Disorder \|Special Senses Disorders
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D012678 MeSH: D012678 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants