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Congenital cardiac diverticulum

disorder
SNOMED 718181001CUI C0546315

Overview

Congenital cardiac diverticulum 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.

EKG abnormality
Frequent (30-79%)HP:0003115
Abnormal aortic morphology
Occasional (5-29%)HP:0001679
Abnormal heart rate
Occasional (5-29%)HP:0011675
Abnormality of the diaphragm
Occasional (5-29%)HP:0000775
Absent/underdeveloped sternum
Occasional (5-29%)HP:0006714
Angina pectoris
Occasional (5-29%)HP:0001681
Aortic coarctation
Occasional (5-29%)HP:0001680
Atria septal defect
Occasional (5-29%)HP:0001631
Cardiac anomaly
Occasional (5-29%)HP:0001627
Cardiac insufficiency
Occasional (5-29%)HP:0001635
Chest discomfort
Occasional (5-29%)HP:0100749
Congenital anterior abdominal wall defect
Occasional (5-29%)HP:0010866
Congenital defect of the pericardium
Occasional (5-29%)HP:0011628
Gap between large left and right abdominal muscles
Occasional (5-29%)HP:0001540
Heart tip and four chambers point towards right side of body
Occasional (5-29%)HP:0001651
Left ventricular wall hypertrophy
Occasional (5-29%)HP:0001712
Missed heartbeat
Occasional (5-29%)HP:0006682
Omphalocoele
Occasional (5-29%)HP:0001539
PAPVR
Occasional (5-29%)HP:0010773
PLSVC
Occasional (5-29%)HP:0005301
Pulmonary artery stenosis
Occasional (5-29%)HP:0004415
Skipped heart beat
Occasional (5-29%)HP:0001962
Syncope
Occasional (5-29%)HP:0001279
Transposition of great vessels
Occasional (5-29%)HP:0001669
Umbilical hernia
Occasional (5-29%)HP:0001537
Underdeveloped pulmonary artery
Occasional (5-29%)HP:0004971
VSD
Occasional (5-29%)HP:0001629
Abnormal coronary artery origin
Very rare (1-4%)HP:0011636
Aortic stenosis
Very rare (1-4%)HP:0001650
Bicuspid aortic valve
Very rare (1-4%)HP:0001647

Related Conditions

Congenital abnormality of cardiac ventricle(parent)

Quick Facts

SNOMED CT
718181001
UMLS CUI
C0546315
Fully Specified Name
Congenital cardiac diverticulum (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.