Cytoscape Web
Click node...


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

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


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Idiopathic pulmonary fibrosis

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- UIP
- Usual interstitial pneumonia

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare respiratory disease

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

Epidemiological data:
(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

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

No signs/symptoms info available.