Autoimmune hypoparathyroidism

disorder

SNOMED 75316000CUI C0271865

Overview

Autoimmune hypoparathyroidism 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.

Autoimmune hypoparathyroidism

Always present (100%)HP:0011771

High blood phosphate levels

Very frequent (80-99%)HP:0002905

Low blood calcium levels

Very frequent (80-99%)HP:0002901

Autoimmune antibody positivity

Frequent (30-79%)HP:0030057

Carpal spasm

Frequent (30-79%)HP:6000919

Cataract

Frequent (30-79%)HP:0000518

Chvostek sign

Frequent (30-79%)HP:0031990

Decreased serum PTH

Frequent (30-79%)HP:0031817

Hypercalciuria

Frequent (30-79%)HP:0002150

Hypoaesthesia

Frequent (30-79%)HP:0033748

Paresthesia

Frequent (30-79%)HP:0003401

Abdominal symptom

Occasional (5-29%)HP:0011458

Autoimmunity

Occasional (5-29%)HP:0002960

Basal ganglion calcification

Occasional (5-29%)HP:0002135

Calcium nephrolithiasis

Occasional (5-29%)HP:0004724

Chest discomfort

Occasional (5-29%)HP:0100749

Confusion

Occasional (5-29%)HP:0001289

Conjunctivitis

Occasional (5-29%)HP:0000509

Depressive episode

Occasional (5-29%)HP:0000716

Excessive, persistent worry and fear

Occasional (5-29%)HP:0000739

Extrapyramidal dysfunction

Occasional (5-29%)HP:0002071

Hair loss

Occasional (5-29%)HP:0001596

Hypocalcemic tetany

Occasional (5-29%)HP:0003472

Hyporeflexia

Occasional (5-29%)HP:0001265

Increased bone mineral density

Occasional (5-29%)HP:0011001

Irritable mood

Occasional (5-29%)HP:0000737

Laryngospasm

Occasional (5-29%)HP:0025425

Long Q-T syndrome

Occasional (5-29%)HP:0001657

Mucocutaneous candidiasis

Occasional (5-29%)HP:0002728

Muscle spasm

Occasional (5-29%)HP:0003394

Related Conditions

Polyglandular autoimmune syndrome, type 1(child)

Autoimmune endocrine disease(parent)

Hypoparathyroidism(parent)

Quick Facts

SNOMED CT: 75316000
UMLS CUI: C0271865
Fully Specified Name: Autoimmune hypoparathyroidism (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.