Prostate cancer, hereditary, 13

Preferred Label : Prostate cancer, hereditary, 13;

Symbol : HPC13;

CISMeF acronym : HPC13;

Type : Phenotype, molecular basis known;

Prefixed ID : #611928;

Details

Origin ID

611928;

UMLS CUI

C2677821;

Automatic exact mappings (from CISMeF team)
- MSMB wt Allele [NCIt concept]
- Pontocerebellar hypoplasia type 13 [ORDO Disease]
Currated CISMeF NLP mapping
- prostate cancer, hereditary, 13 [MeSH concept]
- prostate cancer, hereditary, 13 [MeSH Supplementary Concept]
DO Cross reference
- prostate cancer [DO Concept]
Genes related to phenotype
- Microseminoprotein, beta [OMIM gene]
ORDO concept(s)
- Familial prostate cancer [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- prostate cancer, hereditary, 13 [MeSH Supplementary Concept]
- prostate cancer, hereditary, 13 [MeSH concept]

Keyword's position in hierarchy(ies) :

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