Hyperandrogenism due to cortisone reductase deficiency

disorder

SNOMED 783696009CUI C4329210

Overview

Hyperandrogenism due to cortisone reductase deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal circulating deoxycorticosterone level

Frequent (30-79%)HP:0031186

Congenital adrenal hyperplasia

Frequent (30-79%)HP:0008258

Elevated serum 11-deoxycortisol

Frequent (30-79%)HP:0025436

High blood pressure

Frequent (30-79%)HP:0000822

Increased circulating androgen concentration

Frequent (30-79%)HP:0030348

Menstrual irregularity

Frequent (30-79%)HP:0000858

Decreased circulating renin level

Occasional (5-29%)HP:0003351

Low blood potassium levels

Occasional (5-29%)HP:0002900

Precocious puberty

Occasional (5-29%)HP:0000826

Premature adrenarche

Occasional (5-29%)HP:0012412

Related Conditions

Reproductive system hereditary disorder(parent)

Autosomal hereditary disorder(parent)

Adrenogenital disorder(parent)

Hyperandrogenism(parent)

Hereditary disorder of endocrine system(parent)

Quick Facts

SNOMED CT: 783696009
UMLS CUI: C4329210
Fully Specified Name: Hyperandrogenism due to cortisone reductase deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.