All terms in MONDO
| Label |
Id |
Description |
|
carnitine palmitoyltransferase II deficiency
|
MONDO_0015515 |
|
|
autosomal recessive early-onset Parkinson disease 23
|
MONDO_0014796 |
|
|
young-onset Parkinson disease
|
MONDO_0017279 |
|
|
lateral semicircular canal malformation, familial, with external and middle ear abnormalities
|
MONDO_0012133 |
|
|
myoclonic epilepsy, juvenile, susceptibility to, 3
|
MONDO_0012134 |
|
|
exercise intolerance, riboflavin-responsive
|
MONDO_0014795 |
|
|
macular dystrophy, retinal, 3
|
MONDO_0012139 |
|
|
Carney complex - trismus - pseudocamptodactyly syndrome
|
MONDO_0012137 |
|
|
Carney complex
|
MONDO_0015285 |
|
|
muscular dystrophy-dystroglycanopathy type B6
|
MONDO_0012138 |
|
|
cataract 45
|
MONDO_0014799 |
|
|
TMEM199-CDG
|
MONDO_0014790 |
|
|
Meier-Gorlin syndrome 6
|
MONDO_0014794 |
|
|
metaphyseal undermodeling, spondylar dysplasia, and overgrowth
|
MONDO_0012131 |
|
|
colorectal cancer, susceptibility to, 1
|
MONDO_0012132 |
|
|
microcephaly-congenital cataract-psoriasiform dermatitis syndrome
|
MONDO_0014793 |
|
|
Paget disease of bone 6
|
MONDO_0014792 |
|
|
bone Paget disease
|
MONDO_0005382 |
|
|
myofibrillar myopathy 2
|
MONDO_0012130 |
|
|
Luscan-Lumish syndrome
|
MONDO_0014791 |
|
