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Hereditary arterial and articular multiple calcification syndrome

disorder
SNOMED 718602007CUI C1859372

Overview

Hereditary arterial and articular multiple calcification syndrome 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.

Femoral arterial calcification
Always present (100%)HP:0031303
Iliac arterial calcification
Always present (100%)HP:0031304
Intermittent claudication
Always present (100%)HP:0004417
Abnormal cardiovascular system physiology
Very frequent (80-99%)HP:0011025
Abnormal vascular morphology
Very frequent (80-99%)HP:0025015
Arterial calcification
Very frequent (80-99%)HP:0003207
Arterial occlusion
Very frequent (80-99%)HP:0025324
Tibial arterial calcification
Very frequent (80-99%)HP:0031305
Decreased serum creatinine
Frequent (30-79%)HP:0012101
Arterial tortuosity
Occasional (5-29%)HP:0005116
Coronary artery calcification
Occasional (5-29%)HP:0001717
Ectopic bone formation
HP:0011986
Intervertebral disk calcification
HP:0005645
Periarticular calcification
HP:0025477

Quick Facts

SNOMED CT
718602007
UMLS CUI
C1859372
Fully Specified Name
Hereditary arterial and articular multiple calcification syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
14
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.