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.
esophagus ulcer disease
|
44782 |
|
metopic ridging-ptosis-facial dysmorphism syndrome
|
44715 |
|
SIN3A-related intellectual disability syndrome due to a point mutation
|
44700 |
|
TBC1D24 autosomal dominant nonsyndromic deafness
|
14470 |
|
deafness, autosomal dominant type 65
|
14470 |
|
perihilar bile duct carcinoma
|
44788 |
|
combined immunodeficiency due to GINS1 deficiency
|
44725 |
|
lactic acidemia due to defect in lipoyl-containing component x of the pyruvate dehydrogenase complex
|
C565447 |
|
contagious pustular dermatitides
|
D004474 |
|
thyroid gland differentiated carcinoma
|
15447 |
|
anhidrotic ectodermal dysplasias
|
D004476 |
|
anhydrotic ectodermal dysplasias
|
D004476 |
|
hidrotic ectodermal dysplasias
|
D004476 |
|
hydrotic ectodermal dysplasias
|
D004476 |
|
detrusor sphincter dyssynergia
|
1447 |
|