All terms in MONDO
| Label |
Id |
Description |
|
neuronal ceroid lipofuscinosis 7
|
MONDO_0012588 |
|
|
Pitt-Hopkins syndrome
|
MONDO_0012589 |
|
|
interstitial lung disease due to ABCA3 deficiency
|
MONDO_0012582 |
|
|
tooth agenesis, selective, 5
|
MONDO_0012583 |
|
|
quantitative and/or qualitative congenital phagocyte defect
|
MONDO_0015133 |
|
|
osteogenesis imperfecta type 8
|
MONDO_0012581 |
|
|
von Willebrand disease (hereditary or acquired)
|
MONDO_0024574 |
|
|
immunodeficiency-related disorder
|
MONDO_0024572 |
|
|
hyperparathyroidism 4
|
MONDO_0024570 |
|
|
familial isolated hyperparathyroidism
|
MONDO_0015027 |
|
|
prostate cancer, hereditary, 9
|
MONDO_0012597 |
|
|
fibromatosis, gingival, 4
|
MONDO_0012598 |
|
|
leprosy, susceptibility to, 4
|
MONDO_0012595 |
|
|
PSAT deficiency
|
MONDO_0012596 |
|
|
hypertension, essential, susceptibility to, 8
|
MONDO_0012599 |
|
|
XFE progeroid syndrome
|
MONDO_0012590 |
|
|
brain-lung-thyroid syndrome
|
MONDO_0012593 |
|
|
complement factor I deficiency
|
MONDO_0012594 |
|
|
osteogenesis imperfecta type 5
|
MONDO_0012591 |
|
|
osteogenesis imperfecta type 11
|
MONDO_0012592 |
|
