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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 ..Paralysis (D010243)
Child Nodes:
........Facial Paralysis (D005158) 6
........Gastroparesis (D018589)
........Hemiplegia (D006429) 1
........Ophthalmoplegia (D009886) 41
........Paraplegia (D010264) 14
........Pseudobulbar Palsy (D020828) 1
........Quadriplegia (D011782) 4
........Respiratory Paralysis (D012133)
........Vocal Cord Paralysis (D014826) 6
........Wells Jankovic syndrome (C536692)
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:	8598
Name:	Paralysis
Definition:	A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45)
Alternative IDs:
ParentIDs:	MESH:D009461
TreeNumbers:	C10.597.622 \|C23.888.592.636
Synonyms:	Palsies \|Palsy \|Paralyses \|Paralysis, Todd \|Paralysis, Todd's \|Plegia \|Plegias \|Todd Paralysis \|Todd's Paralysis \|Todds Paralysis
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D010243 MeSH: D010243 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants