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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 ..Paresis (D010291)
Child Nodes:
........Encephalopathy, Spastic Tetraparesis, and Hypogonadism (C565722)
........Hhhh Syndrome (C564411)
........Paraparesis (D020335) 7
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:	8642
Name:	Paresis
Definition:	A general term referring to a mild to moderate degree of muscular weakness, occasionally used as a synonym for PARALYSIS (severe or complete loss of motor function). In the older literature, paresis often referred specifically to paretic neurosyphilis (see NEUROSYPHILIS). 'General paresis' and 'general paralysis' may still carry that connotation. Bilateral lower extremity paresis is referred to as PARAPARESIS.
Alternative IDs:
ParentIDs:	MESH:D009461
TreeNumbers:	C10.597.636 \|C23.888.592.643
Synonyms:	Brachial Pareses \|Brachial Paresis \|Crural Pareses \|Crural Paresis \|Extremity Pareses, Lower \|Extremity Pareses, Upper \|Extremity Paresis, Lower \|Extremity Paresis, Upper \|Hemipareses \|Hemiparesis \|Lower Extremity Pareses \|Lower Extremity Paresis \|Monopareses \|Monopa
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D010291 MeSH: D010291 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants