All terms in MONDO
| Label |
Id |
Description |
|
acquired torsion dystonia
|
MONDO_0044870 |
|
|
dystonia, focal, task-specific
|
MONDO_0044871 |
|
|
lymphatic malformation 9
|
MONDO_0030270 |
|
|
acute annular outer retinopathy
|
MONDO_0017299 |
|
|
combined oxidative phosphorylation deficiency 55
|
MONDO_0859228 |
|
|
cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism
|
MONDO_0859229 |
|
|
glycerol kinase deficiency, juvenile form
|
MONDO_0017295 |
|
|
intellectual disability and myopathy syndrome
|
MONDO_0859224 |
|
|
glycerol kinase deficiency, adult form
|
MONDO_0017296 |
|
|
neurodevelopmental disorder with or without variable movement or behavioral abnormalities
|
MONDO_0859225 |
|
|
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
|
MONDO_0017297 |
|
|
acute zonal occult outer retinopathy
|
MONDO_0017298 |
|
|
reversible cerebral vasoconstriction syndrome
|
MONDO_0017291 |
|
|
Ferguson-Bonni neurodevelopmental syndrome
|
MONDO_0859220 |
|
|
well-differentiated fetal adenocarcinoma of the lung
|
MONDO_0017292 |
|
|
Yoon-Bellen neurodevelopmental syndrome
|
MONDO_0859221 |
|
|
obsolete small cell carcinoma of the bladder
|
MONDO_0017293 |
|
|
glycerol kinase deficiency, infantile form
|
MONDO_0017294 |
|
|
congenital disorder of glycosylation, type Iw, autosomal dominant
|
MONDO_0859223 |
|
|
pontocerebellar hypoplasia, type 1E
|
MONDO_0030260 |
|
