All terms in MONDO
| Label | Id | Description |
|---|---|---|
| congenital factor XI deficiency | MONDO_0012897 | |
| factor XI deficiency | MONDO_0020587 | |
| intellectual disability, X-linked 14 | MONDO_0010236 | |
| immature extragonadal teratoma | MONDO_0024857 | |
| pontocerebellar hypoplasia type 2B | MONDO_0012890 | |
| pontocerebellar hypoplasia type 2C | MONDO_0012891 | |
| mixed teratoma and seminoma | MONDO_0024861 | |
| obsolete treatment for disease | MONDO_0022200 | |
| small size posterior uveal melanoma | MONDO_0024863 | |
| posterior uveal melanoma | MONDO_0003927 | |
| obsolete has treatment by surgery | MONDO_0022201 | |
| locational disease characteristic | MONDO_0045040 | |
| medium/large size posterior uveal melanoma | MONDO_0024864 | |
| hearing loss, X-linked 3 | MONDO_0010228 | |
| retinitis pigmentosa 3 | MONDO_0010227 | |
| hereditary fructose intolerance | MONDO_0009249 | |
| sarcoidosis, susceptibility to, 3 | MONDO_0012889 | |
| fructose and galactose intolerance | MONDO_0009248 | |
| alopecia, congenital | MONDO_0010229 | |
| alopecia totalis | MONDO_0019080 |