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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: Genital Neoplasms, Male (D005834)
Parent Node: Penile Diseases (D010409)
..Starting node ..Penile Neoplasms (D010412)
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:	8774
Name:	Penile Neoplasms
Definition:	Cancers or tumors of the PENIS or of its component tissues.
Alternative IDs:
ParentIDs:	MESH:D005834\|MESH:D010409
TreeNumbers:	C04.588.945.440.715 \|C12.294.260.500 \|C12.294.494.591 \|C12.758.409.500
Synonyms:	Cancer of Penis \|Cancer of the Penis \|Cancer, Penile \|Cancer, Penis \|Cancers, Penile \|Cancers, Penis \|Neoplasm, Penile \|Neoplasm, Penis \|Neoplasms, Penile \|Neoplasms, Penis \|Penile Cancer \|Penile Cancers \|Penile Neoplasm \|Penis Cancer \|Penis Cancers \|Penis Neoplasm \|Pen
Slim Mappings:	Cancer\|Urogenital disease (male)
Reference:	MedGen: D010412 MeSH: D010412 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants