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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
3 OMIM references -
3 associated genes
No signs/symptoms info
Idiopathic pulmonary fibrosis
Frontotemporal dementia with motor neuron disease

ATP11A C9ORF72
DPP9 FUS
DSP TARDBP
FAM13A
MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
TERC
TERC
(0.63)
(0.63)
(0.63)
TARDBP
FUS
TARDBP



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Frontotemporal dementia with motor neuron disease
C9ORF72 FUS TARDBP



Idiopathic pulmonary fibrosis
Frontotemporal dementia with motor neuron disease

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- FTD-ALS
- FTD-MND
- Frontotemporal dementia with amyotrophic lateral sclerosis

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

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

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: adult
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.