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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 1 (OMIM:300147)
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:

9360

Name:

PROSTATE CANCER, HEREDITARY, X-LINKED 1

Definition:

Alternative IDs:

ParentIDs:

MESH:D011471|MESH:D040181

TreeNumbers:

C04.588.945.440.770/300147 |C12.294.260.750/300147 |C12.294.565.625/300147 |C12.758.409.750/300147 |C16.320.322/300147

Synonyms:

HPCX1 |PCSX |PROSTATE CANCER SUSCEPTIBILITY, X-LINKED

Slim Mappings:

Cancer|Genetic disease (inborn)|Urogenital disease (male)

Reference:

MedGen: 300147
MeSH: 300147
OMIM: 300147;

Genes: HPCX;

Phenotypes

1	HP:0001417	X-linked inheritance
2	HP:0012125	Prostate cancer

Disease Causing ClinVar Variants