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.
lysosomal acid lipase deficiency
|
19148 |
|
liposomal acid lipase deficiency, Wolman type
|
19148 |
|
Jamaican vomiting sickness
|
19140 |
|
autosomal recessive thrombophilia due to PC deficiency
|
19145 |
|
cholesterol ester storage disease
|
19149 |
|
cholesteryl ester storage disease
|
19149 |
|
Jamaican vomiting syndrome
|
19140 |
|
autosomal recessive thrombophilia due to congenital protein C deficiency
|
19145 |
|
severe hereditary thrombophilia due to congenital protein C deficiency
|
19145 |
|
autosomal recessive thrombophilia due to congenital protein S deficiency
|
19144 |
|
severe hereditary thrombophilia due to congenital protein S deficiency
|
19144 |
|
primary familial xanthomatosis
|
19148 |
|
Wolman's or triglyceride storage type III disease
|
19148 |
|
inherited susceptibility to mycobacterial diseases
|
19146.0 |
|
infection, ebola virus
|
D019142 |
|