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1 OMIM reference -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Idiopathic pulmonary fibrosis
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

ATP11A APP
DPP9
DSP
FAM13A
MUC5B
OBFC1
SFTPA1
SFTPA2
SFTPC
TERC
TERT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
OBFC1
TERC
(0.56)
(0.56)
APP
APP



Citations in the biomedical literature:


Idiopathic pulmonary fibrosis
ATP11A DPP9 DSP FAM13A MUC5B OBFC1
SFTPA1 SFTPA2 SFTPC TERC TERT
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Idiopathic pulmonary fibrosis
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- UIP
- Usual interstitial pneumonia

Synonym(s):
- HCHWA, Flemish type

Classification (Orphanet):
- Rare respiratory disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic 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:
(no data available)

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

No signs/symptoms info available.