Disease #01536 (IPF (fibrosis, pulmonary, idiopathic (IPF)), OMIM:178500)
Official abbreviation |
IPF |
Name |
fibrosis, pulmonary, idiopathic (IPF) |
OMIM ID |
178500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
51 |
Phenotype entries for this disease |
49 |
Associated with 4 genes |
MUC5B, SFTPA1, SFTPA2, SFTPC |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-02-10 12:49:40 +01:00 (CET) |
Individuals
|