Disease #02760 (MCI1 (myocardial infarction, susceptibility to, type 1 (MCI-1)), OMIM:608446)
Official abbreviation |
MCI1 |
Name |
myocardial infarction, susceptibility to, type 1 (MCI-1) |
OMIM ID |
608446 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
41 |
Phenotype entries for this disease |
2 |
Associated with 12 genes |
ESR1, F13A1, F7, GCLC, GCLM, ITGB3, LGALS2, LTA, MIAT, OLR1, PSMA6, TNFSF4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|