Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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 ..Gait Disorders, Neurologic (D020233)
Child Nodes:
........Gait Apraxia (D020235)
........Gait Ataxia (D020234)
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:	4472
Name:	Gait Disorders, Neurologic
Definition:	Gait abnormalities that are a manifestation of nervous system dysfunction. These conditions may be caused by a wide variety of disorders which affect motor control, sensory feedback, and muscle strength including: CENTRAL NERVOUS SYSTEM DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; or MUSCULAR DISEASES.
Alternative IDs:
ParentIDs:	MESH:D009461
TreeNumbers:	C10.597.404 \|C23.888.592.413
Synonyms:	Ambulation Disorder, Neurologic \|Ambulation Disorders, Neurologic \|Athetotic Gait \|Broadened Gait \|Charcot Gait \|Charcot Gaits \|Charcot's Gait \|Charcots Gait \|Drop Foot Gait \|Duck Gait \|Festinating Gait \|Foot Gait, Drop \|Frontal Gait \|Gait, Athetotic \|Gait, Broadened \|
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D020233 MeSH: D020233 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants