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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
9 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Immunodeficiency due to an early component of complement deficiency

ATP11A C1QA
DPP9 C1QB
DSP C1QC
FAM13A C1R
MUC5B C1S
OBFC1 C2
SFTPA1 C4A
SFTPA2 C4B
SFTPC SERPING1
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SFTPA1
(0.52)
C1QA



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Immunodeficiency due to an early component of complement deficiency
C1QA C1QB C1QC C1R C1S C2
C4A C4B SERPING1



Idiopathic pulmonary fibrosis
Immunodeficiency due to an early component of complement deficiency

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Immunodeficiency due to a C1, C4, or C2 component complement deficiency

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.