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Neonatal acute respiratory distress with surfactant metabolism deficiency
2 OMIM references -
2 associated genes
3 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital pulmonary alveolar proteinosis
Infant acute respiratory distress syndrome
Narcolepsy-cataplexy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare respiratory disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
ABCA3 Q99758601615
SFTPB P07988178640
No signs/symptoms info available.