All terms in MONDO
| Label |
Id |
Description |
|
hypomyelinating leukodystrophy 4
|
MONDO_0012824 |
|
|
inflammatory bowel disease 12
|
MONDO_0012829 |
|
|
scoliosis, isolated, susceptibility to, 5
|
MONDO_0012827 |
|
|
atrial fibrillation, familial, 7
|
MONDO_0012828 |
|
|
inflammatory bowel disease 17
|
MONDO_0012840 |
|
|
epilepsy, childhood absence, susceptibility to, 5
|
MONDO_0012843 |
|
|
primary ciliary dyskinesia 8
|
MONDO_0012844 |
|
|
inflammatory bowel disease 18
|
MONDO_0012841 |
|
|
melanoma, cutaneous malignant, susceptibility to, 7
|
MONDO_0012842 |
|
|
neuronal intestinal dysplasia
|
MONDO_0000858 |
|
|
obsolete Charcot-Marie-Tooth disease type 7
|
MONDO_0000857 |
|
|
obsolete Charcot-Marie-Tooth disease type 6
|
MONDO_0000856 |
|
|
obsolete acromesomelic dysplasia
|
MONDO_0000855 |
|
|
spina bifida occulta
|
MONDO_0000859 |
|
|
obsolete tubular aggregate myopathy
|
MONDO_0000861 |
|
|
obsolete neural tube defect
|
MONDO_0000860 |
|
|
obsolete congenital fiber-type disproportion
|
MONDO_0000865 |
|
|
obsolete congenital myopathy
|
MONDO_0000864 |
|
|
myopathy, lactic acidosis, and sideroblastic anemia
|
MONDO_0000863 |
|
|
obsolete reducing body myopathy
|
MONDO_0000862 |
|
