Cytoscape Web
Click node...


Diffuse panbronchiolitis
1 OMIM reference -
2 associated genes
8 connected diseases
No signs/symptoms info
Disease Type of connection
Idiopathic pulmonary fibrosis
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
1 MeSH reference: C536174

Gene symbol UniProt reference OMIM reference
DPCR1 Q3MIW9613928
MUC5B Q9HC84600770
No signs/symptoms info available.