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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: Sensation Disorders (D012678)
..Starting node ..Somatosensory Disorders (D020886)
Child Nodes:
........Cerebellar Ataxia, Benign, with Thermoanalgesia (C565868)
........Hyperalgesia (D006930)
........Hyperesthesia (D006941)
........Hypesthesia (D006987) 1
........Paresthesia (D010292)
Sister 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
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10345
Name:	Somatosensory Disorders
Definition:	Disorders of sensory information received from superficial and deep regions of the body. The somatosensory system conveys neural impulses which pertain to proprioception, tactile sensation, thermal sensation, pressure sensation, and pain. PERIPHERAL NERVOUS SYSTEM DISEASES; SPINAL CORD DISEASES; and BRAIN DISEASES may be associated with impaired or abnormal somatic sensation.
Alternative IDs:
ParentIDs:	MESH:D012678
TreeNumbers:	C10.597.751.791 \|C23.888.592.763.770
Synonyms:	Diminished, Pain Sensation \|Diminished, Pinprick Sensation \|Diminisheds, Pain Sensation \|Diminisheds, Pinprick Sensation \|Impairment, Light Touch Sensation \|Light Touch Sensation Impairment \|Pain Sensation Diminished \|Pain Sensation Diminisheds \|Pinprick Sensati
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D020886 MeSH: D020886 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants