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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: Connective Tissue Diseases (D003240)
Parent Node: Penile Diseases (D010409)
..Starting node ..Penile Induration (D010411)
Child Nodes:
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:	8773
Name:	Penile Induration
Definition:	A condition characterized by hardening of the PENIS due to the formation of fibrous plaques on the dorsolateral aspect of the PENIS, usually involving the membrane (tunica albuginea) surrounding the erectile tissue (corpus cavernosum penis). This may eventually cause a painful deformity of the shaft or constriction of the urethra, or both.
Alternative IDs:
ParentIDs:	MESH:D003240\|MESH:D010409
TreeNumbers:	C12.294.494.508 \|C17.300.715
Synonyms:	Cavernitides, Fibrous \|Cavernitis, Fibrous \|Fibromatosis, Penile \|Fibrous Cavernitides \|Fibrous Cavernitis \|Penile Fibromatosis \|Peyronie Disease \|Peyronie's Disease \|Peyronies Disease \|Plastic Induration of the Penis
Slim Mappings:	Connective tissue disease\|Urogenital disease (male)
Reference:	MedGen: D010411 MeSH: D010411 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants