Polycystic ovary syndrome 1

Preferred Label : Polycystic ovary syndrome 1;

Symbol : PCOS1;

CISMeF acronym : PCO; PCO1; PCOS1;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Stein-leventhal syndrome; Pco1; PCO; HYPERANDROGENEMIA; PCOS;

Inheritance : Autosomal dominant; probably heterogeneous;

Prefixed ID : %184700;

Details

Origin ID

184700;

UMLS CUI

C0032460;

Automatic exact mappings (from CISMeF team)
- Androgen Excess [NCIt concept]
- Hyperandrogenaemia [MedDRA LLT]
- Polycystic ovary [ICD-11 Subcategory]
- polycystic ovary syndrome [MedlinePlus Topic]
- polycystic ovary syndrome 1 [HGNC gene]
Currated CISMeF NLP mapping
- Androgen excess [ICD-10 Sub-category]
- Hyperandrogenemia [MedDRA LLT]
- Hyperandrogenemia (finding) [SNOMED CT concept]
- Hyperandrogenism [MedDRA Preferred Term]
- Hyperandrogenism [PASCAL descriptor]
- Polycystic Ovary Syndrome [NCIt concept]
- Polycystic Ovary Syndrome [NCIt concept]
- Polycystic ovarian syndrome [ICD-10 Sub-category]
- Polycystic ovarian syndrome [ORDO Disease]
- Polycystic ovarian syndrome [MedDRA LLT]
- Polycystic ovarian syndrome [ICD-10 Sub-category (who)]
- Polycystic ovaries [MedDRA Preferred Term]
- Polycystic ovaries [ICD-9 code]
- Polycystic ovaries [HPO term]
- Polycystic ovaries (disorder) [Inactive SNOMED CT concept]
- Polycystic ovary [PASCAL descriptor]
- Polycystic ovary syndrome [ICD-11 Subcategory]
- Stein-Leventhal syndrome [TUV Concept]
- Stein-Leventhal syndrome [MedDRA LLT]
- hyperandrogenemia [Disease (Nov.)]
- hyperandrogenism [MeSH Descriptor]
- hyperandrogenism [MeSH concept]
- ovary polycystic disorder [Disease (Nov.)]
- polycystic ovaries [SNOMED Notion]
- polycystic ovary syndrome [DO Concept]
- polycystic ovary syndrome [MeSH Descriptor]
- polycystic ovary syndrome [MeSH concept]
DO Cross reference
- polycystic ovary syndrome [DO Concept]
False automatic mappings
- Prostate Cancer Outcomes Study [NCIt concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Amenorrhea [HPO term]
- Autosomal dominant inheritance [HPO term]
- Enlarged polycystic ovaries [HPO term]
- Hirsutism [HPO term]
- Obesity [HPO term]
- Oligomenorrhea [HPO term]
ORDO concept(s)
- Polycystic ovarian syndrome [ORDO Disease]
See also inter- (CISMeF)
- ovarian cysts [MedlinePlus Topic]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Polycystic Ovary Syndrome [NCIt concept]
- Polycystic Ovary Syndrome [NCIt concept]
- Polycystic ovarian syndrome [ICD-10 Sub-category (who)]
- Polycystic ovarian syndrome [MedDRA LLT]
- Polycystic ovarian syndrome [ICD-10 Sub-category]
- Polycystic ovarian syndrome [ORDO Disease]
- Polycystic ovarian syndrome [MedDRA Preferred Term]
- Polycystic ovaries [MedDRA Preferred Term]
- Polycystic ovaries [ICD-9 code]
- Polycystic ovaries [HPO term]
- Polycystic ovaries (disorder) [Inactive SNOMED CT concept]
- Polycystic ovary [MedDRA LLT]
- Polycystic ovary (disorder) [SNOMED CT concept]
- Polycystic ovary syndrome (disorder) [SNOMED CT concept]
- Stein-Leventhal syndrome [MedDRA LLT]
- Stein-Leventhal syndrome [TUV Concept]
- ovary polycystic disorder [Disease (Nov.)]
- polycystic ovaries [SNOMED Notion]
- polycystic ovary syndrome [MeSH Descriptor]
- polycystic ovary syndrome [MeSH concept]
- polycystic ovary syndrome [DO Concept]
- polycystic ovary syndrome [MedlinePlus Topic]

Keyword's position in hierarchy(ies) :

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