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5 OMIM references -
5 associated genes
No signs/symptoms info
COMMON GENES: 2
1 OMIM reference -
2 associated genes
No signs/symptoms info
Congenital pulmonary alveolar proteinosis
Infant acute respiratory distress syndrome

ABCA3 SFTPB
CSF2RA SFTPC
CSF2RB
SFTPB
SFTPC


COMMON
GENES
SFTPB
SFTPC



Citations in the biomedical literature:


Congenital pulmonary alveolar proteinosis
ABCA3 CSF2RA CSF2RB SFTPB SFTPC
Infant acute respiratory distress syndrome



Congenital pulmonary alveolar proteinosis
Infant acute respiratory distress syndrome

Synonym(s):
- Congenital PAP

Synonym(s):
- Hyaline membrane disease
- Infant ARDS
- Infant respiratory distress syndrome
- Neonatal respiratory distress syndrome

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Certain conditions originating in the perinatal period -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic

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

No signs/symptoms info available.