Prolactin deficiency, isolated

Preferred Label : Prolactin deficiency, isolated;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 264110;

Details

Origin ID

264110;

UMLS CUI

C0271586;

Automatic exact mappings (from CISMeF team)
- Prolactin deficiency [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hypoprolactinaemia [MedDRA Preferred Term]
- Hypoprolactinemia [NCIt concept]
- Hypoprolactinemia [MedDRA LLT]
- Isolated prolactin deficiency (disorder) [SNOMED CT concept]
- Reduced circulating prolactin concentration [HPO term]
- hypoprolactinemia [Disease (Nov.)]
- isolated prolactin deficiency [SNOMED Notion]
- prolactin deficiency, isolated [MeSH concept]
- prolactin deficiency, isolated [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Infertility [HPO term]
- Irregular menstruation [HPO term]
- Reduced circulating prolactin concentration [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Hypoprolactinaemia [MedDRA Preferred Term]
- Hypoprolactinemia [MedDRA LLT]
- Hypoprolactinemia [NCIt concept]
- Isolated prolactin deficiency (disorder) [SNOMED CT concept]
- Reduced circulating prolactin concentration [HPO term]
- hypoprolactinemia [Disease (Nov.)]
- isolated prolactin deficiency [SNOMED Notion]
- prolactin deficiency, isolated [MeSH Supplementary Concept]
- prolactin deficiency, isolated [MeSH concept]

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