Prostate cancer

Preferred Label : Prostate cancer;

Type : Phenotype, molecular basis known;

Inheritance : Somatic mutation; Autosomal dominant;

Neoplasia : Early onset prostate cancer;

Prefixed ID : #176807;

Details

Origin ID

176807;

UMLS CUI

C0376358;

Automatic exact mappings (from CISMeF team)
- Familial malignant neoplasm of prostate (disorder) [SNOMED CT concept]
- NCI CTEP SDC Prostate Cancer Sub-Category Terminology [NCIt concept]
- Prostate Cancer Pathway [NCIt concept]
- prostatic neoplasms [MeSH Descriptor]
Currated CISMeF NLP mapping
- Cancer of prostate [MedDRA LLT]
- Carcinoma of prostate (disorder) [SNOMED CT concept]
- Carcinoma prostate [MedDRA LLT]
- Carcinoma prostatic [MedDRA LLT]
- Malignant Prostate Neoplasm [NCIt concept]
- Malignant neoplasm of prostate [ICD-10 category]
- Malignant neoplasm of prostate [MedDRA LLT]
- Malignant neoplasm of prostate [ICD-9 code]
- Malignant neoplasm of prostate [ICD-10 category (who)]
- Malignant neoplasms of prostate [ICD-11 Category]
- Malignant tumor of prostate (disorder) [SNOMED CT concept]
- Primary malignant neoplasm of prostate (disorder) [SNOMED CT concept]
- Prostate Carcinoma [NCIt concept]
- Prostate cancer [HPO term]
- Prostate cancer [PASCAL descriptor]
- Prostate cancer [HPMULTI term]
- Prostate cancer [MedDRA Preferred Term]
- Prostate cancer NOS [MedDRA LLT]
- Prostate carcinoma [MedDRA LLT]
- Prostate carcinoma [PASCAL descriptor]
- Prostatic cancer [MedDRA LLT]
- Prostatic carcinoma [MedDRA LLT]
- Prostatic neoplasms malignant [MedDRA High Level Term]
- malignant neoplasm of prostate [SNOMED Notion]
- malignant neoplasm prostate [ICPC-2 Rubric]
- prostate cancer [Disease (Nov.)]
- prostate cancer [DO Concept]
- prostate cancer [MedlinePlus Topic]
- prostate cancer [MeSH concept]
- prostate cancer [Radlex concept]
- prostate carcinoma [DO Concept]
DO Cross reference
- prostate cancer [DO Concept]
Genes related to phenotype
- Androgen receptor [OMIM gene]
- Brca2 dna repair-associated protein [OMIM gene]
- Cadherin 1 [OMIM gene]
- Checkpoint kinase 2 [OMIM gene]
- Kruppel-like factor 6 [OMIM gene]
- Max-interacting protein 1 [OMIM gene]
- Mitotic arrest deficient 1 like 1 [OMIM gene]
- Phosphatase and tensin homolog [OMIM gene]
- Zinc finger homeobox 3 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Prostate cancer [HPO term]
- Somatic mutation [HPO term]
ORDO concept(s)
- Familial prostate cancer [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Cancer of prostate [MedDRA LLT]
- Malignant Prostate Neoplasm [NCIt concept]
- Malignant neoplasm of prostate [ICD-10 category (who)]
- Malignant neoplasm of prostate [ICD-9 code]
- Malignant neoplasm of prostate [MedDRA LLT]
- Malignant neoplasm of prostate [ICD-10 category]
- Malignant tumor of prostate (disorder) [SNOMED CT concept]
- Prostate cancer [MedDRA Preferred Term]
- Prostate cancer [HPO term]
- Prostate cancer NOS [MedDRA LLT]
- Prostatic cancer [MedDRA LLT]
- Prostatic neoplasms malignant [MedDRA High Level Term]
- malignant neoplasm of prostate [SNOMED Notion]
- malignant neoplasm prostate [ICPC-2 Rubric]
- prostate cancer [MeSH concept]
- prostate cancer [MedlinePlus Topic]
- prostate cancer [Disease (Nov.)]
Validated automatic mappings to BTNT
- prostate carcinoma [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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