CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C2931838 | Familial HDL deficiency | DO | Tangier disease | 1388 |
C2931838 | Familial HDL deficiency | MONDO | apolipoprotein A-I deficiency | 0011393 |
C2931838 | Familial HDL deficiency | MSH | Familial HDL deficiency | C538394 |
C2931838 | Familial HDL deficiency | MSH | Hdl Deficiency, Type 2 | C538394 |
C2931838 | Familial HDL deficiency | OMIM | HYPOALPHALIPOPROTEINEMIA, PRIMARY | 604091 |
C2931838 | Familial HDL deficiency | OMIM | HYPOALPHALIPOPROTEINEMIA, FAMILIAL | 604091 |
C2931838 | Familial HDL deficiency | OMIM | FAMILIAL HDL DEFICIENCY | 604091 |
C2931838 | Familial HDL deficiency | ORDO | Apolipoprotein A-I deficiency | 425 |