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Congenital pulmonary alveolar capillary dysplasia

disorder
SNOMED 708028001CUI C2677362

Overview

Congenital pulmonary alveolar capillary dysplasia 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.

Laboured breathing
Very frequent (80-99%)HP:0002098
Pulmonary artery hypertension
Very frequent (80-99%)HP:0002092
Intestinal malrotation
Frequent (30-79%)HP:0002566
Left ventricular hypoplasia
Frequent (30-79%)HP:0004383
PDA
Frequent (30-79%)HP:0001643
2 vessel cord
Occasional (5-29%)HP:0001195
Absent anus
Occasional (5-29%)HP:0002023
Absent gallbladder
Occasional (5-29%)HP:0011467
Absent spleen
Occasional (5-29%)HP:0001746
Aganglionic megacolon
Occasional (5-29%)HP:0002251
Annular pancreas
Occasional (5-29%)HP:0001734
Aortic stenosis
Occasional (5-29%)HP:0001650
Atria septal defect
Occasional (5-29%)HP:0001631
Atrioventricular septal defect
Occasional (5-29%)HP:0006695
Bicuspid aortic valve
Occasional (5-29%)HP:0001647
Duodenal stenosis
Occasional (5-29%)HP:0100867
Hydronephrosis
Occasional (5-29%)HP:0000126
Multiple vertebral anomalies
Occasional (5-29%)HP:0003468
Pulmonary valve atresia
Occasional (5-29%)HP:0010882
Tetrology of fallot
Occasional (5-29%)HP:0001636
Tracheoesophageal fistula
Occasional (5-29%)HP:0002575
Volvulus
Occasional (5-29%)HP:0002580
VSD
Occasional (5-29%)HP:0001629

Related Conditions

Dysplasia of lung(parent)

Quick Facts

SNOMED CT
708028001
UMLS CUI
C2677362
Fully Specified Name
Congenital pulmonary alveolar capillary dysplasia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
23
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.