All terms in MONDO
| Label |
Id |
Description |
|
inflammatory diarrhea
|
MONDO_0000252 |
|
|
gastrointestinal mucositis
|
MONDO_0000888 |
|
|
diarrheal disease secondary to altered bowel motility
|
MONDO_0000251 |
|
|
osmotic diarrheal disease
|
MONDO_0000250 |
|
|
non-infectious diarrheal disease
|
MONDO_0045030 |
|
|
developmental and epileptic encephalopathy, 3
|
MONDO_0012245 |
|
|
spastic paraparesis-cataracts-speech delay syndrome
|
MONDO_0036212 |
|
|
spinocerebellar ataxia type 26
|
MONDO_0012246 |
|
|
B-cell immunodeficiency, distal limb anomalies, and urogenital malformations
|
MONDO_0012243 |
|
|
prostate cancer, hereditary, 5
|
MONDO_0012244 |
|
|
Lynch syndrome 2
|
MONDO_0012249 |
|
|
lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation
|
MONDO_0036217 |
|
|
pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal
|
MONDO_0032931 |
|
|
lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster
|
MONDO_0036218 |
|
|
spinocerebellar ataxia type 27
|
MONDO_0012247 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2K
|
MONDO_0012248 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
|
MONDO_0012241 |
|
|
syncope, familial vasovagal
|
MONDO_0012242 |
|
|
nemaline myopathy 4
|
MONDO_0012240 |
|
|
typical nemaline myopathy
|
MONDO_0015737 |
|