Congenital pulmonary alveolar proteinosis

disorder

SNOMED 707442002CUI C2931035

Overview

Congenital pulmonary alveolar proteinosis 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.

Abnormal circulating protein level

Very frequent (80-99%)HP:0010876

Crazy-paving pattern

Frequent (30-79%)HP:0025391

Failure to thrive in first year of life

Frequent (30-79%)HP:0001531

Hypoxia

Frequent (30-79%)HP:0012418

Laboured breathing

Frequent (30-79%)HP:0002098

Respiratory distress requiring endotracheal intubation

Frequent (30-79%)HP:0004887

Restrictive lung disease

Frequent (30-79%)HP:0002091

Acute infectious pneumonia

Occasional (5-29%)HP:0011949

Autoimmune antibody positivity

Occasional (5-29%)HP:0030057

Coughing

Occasional (5-29%)HP:0012735

Elevated carcinoembryonic antigen level

Occasional (5-29%)HP:0031029

Foamy macrophages

Occasional (5-29%)HP:0003651

Racing heart

Occasional (5-29%)HP:0001649

Rales

Occasional (5-29%)HP:0030830

Tachypnea

Occasional (5-29%)HP:0002789

Related Conditions

Congenital disease(parent)

Pulmonary alveolar proteinosis(parent)

Perinatal respiratory disorders(parent)

Quick Facts

SNOMED CT: 707442002
UMLS CUI: C2931035
Fully Specified Name: Congenital pulmonary alveolar proteinosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.