All terms in MONDO
| Label |
Id |
Description |
|
familial hyperinsulinism
|
MONDO_0017182 |
|
|
panic disorder 3
|
MONDO_0012384 |
|
|
metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands
|
MONDO_0012385 |
|
|
hyperinsulinemic hypoglycemia, familial, 4
|
MONDO_0012382 |
|
|
diazoxide-sensitive diffuse hyperinsulinism
|
MONDO_0015624 |
|
|
primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
|
MONDO_0012383 |
|
|
circadian rhythm sleep disorder, delayed sleep phase type
|
MONDO_0024377 |
|
|
sleep disorder, initiating and maintaining sleep
|
MONDO_0024376 |
|
|
circadian rhythm sleep disorder, irregular sleep wake type
|
MONDO_0024379 |
|
|
circadian rhythm sleep disorder, advanced sleep phase type
|
MONDO_0024378 |
|
|
complex cortical dysplasia with other brain malformations 7
|
MONDO_0012399 |
|
|
brachydactyly, coloboma, and anterior segment dysgenesis
|
MONDO_0012397 |
|
|
retinal cone dystrophy 3A
|
MONDO_0012398 |
|
|
neuronal ceroid lipofuscinosis 8 northern epilepsy variant
|
MONDO_0012391 |
|
|
neuronal ceroid lipofuscinosis 8
|
MONDO_0010830 |
|
|
2-methylbutyryl-CoA dehydrogenase deficiency
|
MONDO_0012392 |
|
|
arthrogryposis multiplex with deafness, inguinal hernias, and early death
|
MONDO_0012390 |
|
|
cataract 18
|
MONDO_0012395 |
|
|
exercise-induced hyperinsulinism
|
MONDO_0012396 |
|
|
disorder of carbohydrate transmembrane transport and absorption
|
MONDO_0017706 |
|
