| 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.
|
reductase deficiency, 7-dehydrocholesterol
|
D019082 |
|
|
rutledge friedman harrod syndrome
|
D019082 |
|
|
7-dehydrocholesterol reductase deficiencies
|
D019082 |
|
|
hyperotosis corticalis generalisata familiaris
|
D019082 |
|
|
smith lemli opitz syndrome
|
D019082 |
|
|
acrodysgenital syndrome, lethal
|
D019082 |
|
|
acrodysgenital syndromes, lethal
|
D019082 |
|
|
rutledge lethal multiple congenital anomaly syndrome
|
D019082 |
|
|
Senile dermatitis herpetiformis
|
19082 |
|
|
smith lemli opitz syndrome, type 1
|
D019082 |
|
|
smith lemli opitz syndrome, type 2
|
D019082 |
|
|
smith lemli opitz syndrome, type II
|
D019082 |
|
|
smith lemli opitz syndrome, type i
|
D019082 |
|
|
RSH SLO syndrome
|
D019082 |
|
|
sex reversal, renal hypoplasia, and unilobar lung polydactyly
|
D019082 |
|
