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1 OMIM reference -
11 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 3
Idiopathic pulmonary fibrosis
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

ATP11A CTNNA3
DPP9 DSC2
DSP DSG2
FAM13A DSP
MUC5B JUP
OBFC1 LMNA
SFTPA1 PKP2
SFTPA2 RYR2
SFTPC TGFB3
TERC TMEM43
TERT TTN


COMMON
GENES
DSP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
DSP
DSP
(0.89)
(0.77)
(0.56)
JUP
PKP2
DSC2



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
CTNNA3 DSC2 DSG2 JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Idiopathic pulmonary fibrosis
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, classic form
- Familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form
- Familial isolated arrhythmogenic ventricular dysplasia, classic form

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Diseases of the circulatory 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:
(no data available)

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

No signs/symptoms info available.