Autosomal dominant primary hypomagnesemia with hypocalciuria

disorder

SNOMED 725393000CUI C1835171

Overview

Autosomal dominant primary hypomagnesemia with hypocalciuria 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.

Hypomagnesemia

Always present (100%)HP:0002917

Renal magnesium wasting

Always present (100%)HP:0005567

Low blood potassium levels

Frequent (30-79%)HP:0002900

Low urine calcium levels

Frequent (30-79%)HP:0003127

Renal failure

Occasional (5-29%)HP:0000083

Calcium deposits in joints

HP:0000934

Muscle weakness, generalised

HP:0003324

Seizures

HP:0001250

Related Conditions

Autosomal dominant hereditary disorder(parent)

Primary hypomagnesemia(parent)

Hypocalciuria(parent)

Quick Facts

SNOMED CT: 725393000
UMLS CUI: C1835171
Fully Specified Name: Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.