Disease #00176 (HDLCD-2 (hypoalphalipoproteinemia (HDL deficiency, type 2 (HDLCD-2))), OMIM:604091)
| Official abbreviation |
HDLCD-2 |
| Name |
hypoalphalipoproteinemia (HDL deficiency, type 2 (HDLCD-2)) |
| OMIM ID |
604091 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
ABCA1, APOA1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-08-11 14:08:14 +02:00 (CEST) |
| Date last edited |
N/A |
|
