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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 5
1 OMIM reference -
6 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Behavioral variant of frontotemporal dementia

ATP11A C9ORF72
DPP9 CHMP2B
DSP GRN
FAM13A MAPT
MUC5B PSEN1
OBFC1 VCP
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
TERC
SFTPC
TERC
DSP
(0.73)
(0.72)
(0.63)
(0.63)
(0.49)
VCP
MAPT
VCP
VCP
PSEN1



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Behavioral variant of frontotemporal dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Idiopathic pulmonary fibrosis
Behavioral variant of frontotemporal dementia

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- bv-FTD

Classification (Orphanet):
- Rare respiratory disease
Classification (Orphanet):
- 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: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.