ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

5 OMIM references -
5 associated genes
No signs/symptoms info

Chronic respiratory distress with surfactant metabolism deficiency

Congenital pulmonary alveolar proteinosis

Citations in the biomedical literature:

Chronic respiratory distress with surfactant metabolism deficiency		Congenital pulmonary alveolar proteinosis
	Synonym(s): (no synonyms)		Synonym(s): - Congenital PAP

	Classification (Orphanet): - Rare genetic disease - Rare respiratory disease		Classification (Orphanet): - Rare genetic disease - Rare respiratory disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the respiratory system -

	Epidemiological data: Class of prevalence: - Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 5 OMIM references - No MeSH references

No signs/symptoms info available.