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
|