Disease #06903 (LMPHM10 (lymphatic malformation, type 10), OMIM:619369)
| Official abbreviation |
LMPHM10 |
| Name |
lymphatic malformation, type 10 |
| OMIM ID |
619369 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ANGPT2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-03-21 10:04:34 +01:00 (CET) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|