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

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


COMMON
GENES
SFTPC



Citations in the biomedical literature:


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



Idiopathic pulmonary fibrosis
Congenital pulmonary alveolar proteinosis

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Congenital PAP

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

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

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
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 -
1 MeSH reference: D054990
External references:
5 OMIM references -
No MeSH references

No signs/symptoms info available.