Prostate cancer, hereditary, 1

Preferred Label : Prostate cancer, hereditary, 1;

Symbol : HPC1;

CISMeF acronym : HPC1; PRCA1;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : PRCA1;

Inheritance : Autosomal dominant form;

Prefixed ID : #601518;

Details

Origin ID

601518;

UMLS CUI

C4722327;

Automatic exact mappings (from CISMeF team)
- RNASEL wt Allele [NCIt concept]
- hereditary prostate cancer 1 [HGNC gene]
- prostate cancer, familial [MeSH Supplementary Concept]
- syntaxin 1A [ORDO Gene]
CISMeF manual mappings
- autosomal dominant hereditary prostate cancer [Disease (Nov.)]
DO Cross reference
- prostate cancer [DO Concept]
Genes related to phenotype
- Ribonuclease L [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Neoplasm [HPO term]
- Prostate cancer [HPO term]
ORDO concept(s)
- Familial prostate cancer [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Familial malignant neoplasm of prostate (disorder) [SNOMED CT concept]
- Familial prostate cancer [ORDO Disease]
- Hereditary Prostate Carcinoma [NCIt concept]
- Prostate cancer, familial [MeSH concept]
- autosomal dominant hereditary prostate cancer [Disease (Nov.)]
- familial prostate cancer [Disease (Nov.)]
- prostate cancer, familial [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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