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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: Genetic Diseases, X-Linked (D040181)
Parent Node: Prostatic Neoplasms (D011471)
..Starting node ..Prostate Cancer, Hereditary, X-Linked 2 (C567477)
Child Nodes:
Sister Nodes:
..Phyllodes Tumor of the Prostate (C549759)
..Prostate cancer, familial (C537243)
..PROSTATE CANCER, HEREDITARY, 1 (OMIM:601518)
..Prostate Cancer, Hereditary, 10 (C567011)
..Prostate Cancer, Hereditary, 11 (C567449)
..Prostate Cancer, Hereditary, 12 (C567510)
..Prostate Cancer, Hereditary, 13 (C567456)
..Prostate Cancer, Hereditary, 14 (C567448)
..Prostate Cancer, Hereditary, 15 (C567447)
..Prostate Cancer, Hereditary, 3 (C563883)
..Prostate Cancer, Hereditary, 4 (C563882)
..Prostate Cancer, Hereditary, 5 (C563744)
..Prostate Cancer, Hereditary, 6 (C563699)
..Prostate Cancer, Hereditary, 7 (C565201)
..Prostate Cancer, Hereditary, 8 (C566426)
..Prostate Cancer, Hereditary, 9 (C567031)
..PROSTATE CANCER, HEREDITARY, X-LINKED 1 (OMIM:300147)
..Prostate Cancer, Hereditary, X-Linked 2 (C567477)
..PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (OMIM:603688)
..Prostatic Neoplasms, Castration-Resistant (D064129)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9361
Name:	Prostate Cancer, Hereditary, X-Linked 2
Definition:
Alternative IDs:	OMIM:300704
ParentIDs:	MESH:D011471\|MESH:D040181
TreeNumbers:	C04.588.945.440.770/C567477 \|C12.294.260.750/C567477 \|C12.294.565.625/C567477 \|C12.758.409.750/C567477 \|C16.320.322/C567477
Synonyms:	HPCX2
Slim Mappings:	Cancer\|Genetic disease (inborn)\|Urogenital disease (male)
Reference:	MedGen: C567477 MeSH: C567477 OMIM: 300704; Genes:
Phenotypes
Disease Causing ClinVar Variants