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: Spasm (D013035)
..Starting node ..Trismus (D014313)
Child Nodes:
........Crisponi syndrome (C536214)
........Hecht syndrome (C535857)
Sister Nodes:
..Behr syndrome (C537669)
..Dwarfism, Familial, With Muscle Spasms (C563447)
..Hemifacial Spasm (D019569) 1
..Satoyoshi syndrome (C536616)
..Trismus (D014313) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11280
Name:	Trismus
Definition:	Spasmodic contraction of the masseter muscle resulting in forceful jaw closure. This may be seen with a variety of diseases, including TETANUS, as a complication of radiation therapy, trauma, or in association with neoplastic conditions.
Alternative IDs:
ParentIDs:	MESH:D013035
TreeNumbers:	C10.597.613.750.700 \|C23.888.592.608.750.700
Synonyms:	Lockjaw \|Lock Jaw \|Masseter Muscle Spasm \|Masseter Muscle Spasms \|Masseter Spasm \|Masseter Spasms \|Muscle Spasm, Masseter \|Muscle Spasms, Masseter \|Spasm, Masseter \|Spasm, Masseter Muscle \|Spasms, Masseter \|Spasms, Masseter Muscle
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D014313 MeSH: D014313 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants