| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
|
MONDO_bioport_pref_name
|
183,974 entries
|
There is 0 pattern entry.
|
B4GALT7-CDG
|
7526 |
|
|
sclerotylosis
|
C537526 |
|
|
bilateral PPD2
|
17526 |
|
|
XGPT deficiency
|
7526 |
|
|
huriez syndrome
|
C537526 |
|
|
familial hypoadrenocorticism
|
D000075262 |
|
|
familial hypoadrenocorticisms
|
D000075262 |
|
|
hypoadrenocorticisms, familial
|
D000075262 |
|
|
hypoplasia, congenital adrenal
|
D000075262 |
|
|
adrenal hypoplasia, X-linked
|
D000075262 |
|
|
polydactyly of a triphalangeal thumb, bilateral
|
17526 |
|
|
x linked adrenal hypoplasia
|
D000075262 |
|
|
x-linked addison disease
|
D000075262 |
|
|
familial X-linked addison disease
|
D000075262 |
|
|
x linked addison disease
|
D000075262 |
|
