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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: Apraxias (D001072)
Parent Node: Gait Disorders, Neurologic (D020233)
..Starting node ..Gait Apraxia (D020235)
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:	4470
Name:	Gait Apraxia
Definition:	Impaired ambulation not attributed to sensory impairment or motor weakness. FRONTAL LOBE disorders; BASAL GANGLIA DISEASES (e.g., PARKINSONIAN DISORDERS); DEMENTIA, MULTI-INFARCT; ALZHEIMER DISEASE; and other conditions may be associated with gait apraxia.
Alternative IDs:
ParentIDs:	MESH:D001072\|MESH:D020233
TreeNumbers:	C10.597.404.400 \|C10.597.606.881.350.600 \|C23.888.592.413.400 \|C23.888.592.604.882.350.600
Synonyms:	Apraxia, Bruns' Gait \|Apraxia, Frontal Gait \|Apraxia, Gait \|Apraxia of Gait \|Apraxias, Bruns' Gait \|Apraxias, Frontal Gait \|Apraxias, Gait \|Bruns Apraxia, Gait \|Bruns' Apraxia, Gait \|Bruns' Apraxia of Gait \|Bruns Gait Apraxia \|Bruns' Gait Apraxia \|Bruns' Gait Apraxi
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D020235 MeSH: D020235 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants