Cytoscape Web
Click node...


1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 5
3 OMIM references -
3 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

ATP11A HNRNPA1
DPP9 HNRNPA2B1
DSP VCP
FAM13A
MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
TERC
SFTPC
TERC
TERC
(0.73)
(0.72)
(0.63)
(0.63)
(0.63)
VCP
HNRNPA1
VCP
HNRNPA2B1
VCP



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
HNRNPA1 HNRNPA2B1 VCP



Idiopathic pulmonary fibrosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- IBMPFD
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid amyotrophic lateral sclerosis
- Pagetoid neuroskeletal syndrome

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

Classification (ICD10):
- Diseases of the respiratory system -
Classification (ICD10):
- Diseases of the nervous 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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.