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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: Neuromuscular Manifestations (D020879)
..Starting node ..Fasciculation (D005207)
Child Nodes:
........Ataxia with Fasciculations (C566246)
Sister Nodes:
..Fasciculation (D005207) 1
..Muscle Cramp (D009120) 3
..Muscle Hypertonia (D009122) 24
..Muscle Hypotonia (D009123) 30
..Muscle Weakness (D018908) 5
..Muscular Atrophy (D009133) 16
..Myokymia (D020385) 5
..Myotonia (D009222) 2
..Spasm (D013035) 8
..Tetany (D013746)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4193
Name:	Fasciculation
Definition:	Involuntary contraction of the muscle fibers innervated by a motor unit. Fasciculations can often by visualized and take the form of a muscle twitch or dimpling under the skin, but usually do not generate sufficient force to move a limb. They may represent a benign condition or occur as a manifestation of MOTOR NEURON DISEASE or PERIPHERAL NERVOUS SYSTEM DISEASES. (Adams et al., Principles of Neurology, 6th ed, p1294)
Alternative IDs:
ParentIDs:	MESH:D020879
TreeNumbers:	C10.597.613.250 \|C23.888.592.608.250
Synonyms:	Benign Fasciculation \|Benign Fasciculations \|Fasciculation, Benign \|Fasciculation, Muscular \|Fasciculation, Neural \|Fasciculations \|Fasciculations, Benign \|Fasciculation, Skeletal Muscle \|Fasciculations, Muscular \|Fasciculations, Neural \|Fasciculations, Skeletal M
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D005207 MeSH: D005207 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants