Idiopathic hypercalcemia of infancy

disorder

SNOMED 34225008CUI C0268080

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Decreased serum PTH

Always present (100%)HP:0031817

Hypercalcemia

Always present (100%)HP:0003072

Hypercalciuria

Always present (100%)HP:0002150

Medullary nephrocalcinosis

Always present (100%)HP:0012408

Increased urine output

Frequent (30-79%)HP:0000103

Muscular hypotonia

Frequent (30-79%)HP:0001252

Undergrowth

Frequent (30-79%)HP:0001508

Kidney stones

Occasional (5-29%)HP:0000787

Dehydration

HP:0001944

Inactivity

HP:0001254

Nephrocalcinosis

HP:0000121

Vomiting

HP:0002013

Weight loss

HP:0001824

Related Conditions

Idiopathic infantile hypercalcaemia - mild form(child)

Severe idiopathic hypercalcaemia of infancy(child)

Idiopathic hypercalcemia(parent)

Infantile hypercalcemia(parent)

Quick Facts

SNOMED CT: 34225008
UMLS CUI: C0268080
Fully Specified Name: Idiopathic hypercalcemia of infancy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.