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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
7 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Pulverulent cataract

ATP11A CRYBB1
DPP9 CRYGC
DSP GJA3
FAM13A GJA8
MUC5B LIM2
OBFC1 MAF
SFTPA1 VIM
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
(0.78)
VIM



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Pulverulent cataract
CRYBB1 CRYGC GJA3 GJA8 LIM2 MAF
VIM



Idiopathic pulmonary fibrosis
Pulverulent cataract

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- Dusty cataract

Classification (Orphanet):
- Rare respiratory disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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.