All terms in MONDO
| Label |
Id |
Description |
|
Joubert syndrome 29
|
MONDO_0800372 |
|
|
Joubert syndrome
|
MONDO_0018772 |
|
|
carbon monoxide poisoning
|
MONDO_0800373 |
|
|
dyskeratosis congenita, autosomal recessive 7
|
MONDO_0800370 |
|
|
dyskeratosis congenita
|
MONDO_0015780 |
|
|
cardiomyopathy, familial restrictive, 5
|
MONDO_0800371 |
|
|
papular urticaria
|
MONDO_0043254 |
|
|
peroxisome biogenesis disorder, complementation group K
|
MONDO_0800365 |
|
|
peroxisome biogenesis disorder due to PEX14 defect
|
MONDO_0100268 |
|
|
dyskeratosis congenita, autosomal dominant 4
|
MONDO_0800366 |
|
|
Joubert syndrome 19
|
MONDO_0800363 |
|
|
peroxisome biogenesis disorder, complementation group 3
|
MONDO_0800364 |
|
|
peroxisome biogenesis disorder due to PEX12 defect
|
MONDO_0100266 |
|
|
parkinson disease 19B, early-onset
|
MONDO_0800369 |
|
|
juvenile-onset Parkinson disease
|
MONDO_0000828 |
|
|
cardiomyopathy, dilated, 1LL
|
MONDO_0800367 |
|
|
familial dilated cardiomyopathy
|
MONDO_0016333 |
|
|
cardiomyopathy, dilated, 1MM
|
MONDO_0800368 |
|
|
rheumatoid vasculitis
|
MONDO_0043267 |
|
|
autoimmune vasculitis
|
MONDO_0030703 |
|
