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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: Penile Diseases (D010409)
..Starting node ..Priapism (D011317)
Child Nodes:
........Priapism, familial idiopathic (C531791)
Sister Nodes:
..Balanitis (D001446) 1
..Hypospadias (D007021) 17
..MORM syndrome (C536984)
..Penile Induration (D010411)
..Penile Neoplasms (D010412)
..Phimosis (D010688) 2
..Priapism (D011317) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9268
Name:	Priapism
Definition:	A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments.
Alternative IDs:
ParentIDs:	MESH:D010409
TreeNumbers:	C12.294.494.786
Synonyms:	Priapisms
Slim Mappings:	Urogenital disease (male)
Reference:	MedGen: D011317 MeSH: D011317 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants