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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: Cysts (D003560)
Parent Node: Mucinoses (D017520)
..Starting node ..Ganglion Cysts (D045888)
Child Nodes:
Sister Nodes:
..Ganglion Cysts (D045888)
..Mucinosis, Follicular (D000507)
..Mucopolysaccharidoses (D009083) 10
..Myxedema (D009230)
..Scleredema Adultorum (D012592)
..Scleromyxedema (D053718)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4493
Name:	Ganglion Cysts
Definition:	Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE, especially of the hands, wrists, or feet. They are not true cysts as they lack epithelial wall. They are distinguished from SYNOVIAL CYSTS by the lack of communication with a joint cavity or the SYNOVIAL MEMBRANE.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D017520
TreeNumbers:	C04.182.347 \|C17.300.550.274
Synonyms:	Cyst, Ganglion \|Cyst, Ganglionic \|Cyst, Myxoid \|Cysts, Ganglion \|Cysts, Ganglionic \|Cysts, Myxoid \|Ganglion \|Ganglion Cyst \|Ganglionic Cyst \|Ganglionic Cysts \|Ganglions \|Myxoid Cyst \|Myxoid Cysts
Slim Mappings:	Cancer\|Connective tissue disease
Reference:	MedGen: D045888 MeSH: D045888 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants