| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
|
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
|
622,528 entries
|
There is 0 pattern entry.
|
familial alpha-lipoprotein deficiency
|
C0039292 |
|
|
Alpha high density lipoprotein deficiency disease
|
C0039292 |
|
|
Familial high density lipoprotein deficiency disease
|
C0039292 |
|
|
familial high density lipoprotein deficiency disease
|
C0039292 |
|
|
High density lipoprotein deficiency, Tangier type
|
C0039292 |
|
|
high density lipoprotein deficiency, Tangier type
|
C0039292 |
|
|
High density lipoprotein deficiency, type 1
|
C0039292 |
|
|
high density lipoprotein deficiency, type 1
|
C0039292 |
|
|
ATP-binding cassette transporter A1 deficiency
|
C0039292 |
|
|
Defective adenosine triphosphate-binding cassette transporter A1
|
C0039292 |
|
|
defective adenosine triphosphate-binding cassette transporter A1
|
C0039292 |
|
