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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: Ataxia (D001259)
Parent Node: Gait Disorders, Neurologic (D020233)
..Starting node ..Gait Ataxia (D020234)
Child Nodes:
Sister Nodes:
..Gait Apraxia (D020235)
..Gait Ataxia (D020234)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4471
Name:	Gait Ataxia
Definition:	Impairment of the ability to coordinate the movements required for normal ambulation (WALKING) which may result from impairments of motor function or sensory feedback. This condition may be associated with BRAIN DISEASES (including CEREBELLAR DISEASES and BASAL GANGLIA DISEASES); SPINAL CORD DISEASES; or PERIPHERAL NERVOUS SYSTEM DISEASES.
Alternative IDs:
ParentIDs:	MESH:D001259\|MESH:D020233
TreeNumbers:	C10.597.350.090.750 \|C10.597.404.450 \|C23.888.592.350.090.600 \|C23.888.592.413.450
Synonyms:	Ataxia, Cerebellar Gait \|Ataxia, Gait \|Ataxia of Gait \|Ataxias, Cerebellar Gait \|Ataxia, Sensory Gait \|Ataxias, Gait \|Ataxias, Sensory Gait \|Cerebellar Gait \|Cerebellar Gait Ataxia \|Cerebellar Gait Ataxias \|Cerebellar Gaits \|Gait Ataxia, Cerebellar \|Gait Ataxias \|Gai
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D020234 MeSH: D020234 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants