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5 OMIM references -
5 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
11 associated genes
No signs/symptoms info
Congenital pulmonary alveolar proteinosis
Idiopathic pulmonary fibrosis

ABCA3 ATP11A
CSF2RA DPP9
CSF2RB DSP
SFTPB FAM13A
SFTPC MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


COMMON
GENES
SFTPC



Citations in the biomedical literature:


Congenital pulmonary alveolar proteinosis
ABCA3 CSF2RA CSF2RB SFTPB SFTPC
Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 TERC TERT



Congenital pulmonary alveolar proteinosis
Idiopathic pulmonary fibrosis

Synonym(s):
- Congenital PAP

Synonym(s):
- UIP
- Usual interstitial pneumonia

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Diseases of the respiratory system -

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: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
5 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D054990

No signs/symptoms info available.