All terms in MONDO
| Label | Id | Description |
|---|---|---|
| autosomal recessive nonsyndromic hearing loss 83 | MONDO_0013365 | |
| spondylocostal dysostosis 4, autosomal recessive | MONDO_0013366 | |
| hypertrophic cardiomyopathy 7 | MONDO_0013369 | |
| brachyolmia, Maroteaux type | MONDO_0013360 | |
| chromosome 2q31.1 duplication syndrome | MONDO_0013363 | |
| Rubinstein-Taybi syndrome due to EP300 haploinsufficiency | MONDO_0013364 | |
| congenital prothrombin deficiency | MONDO_0013361 | |
| THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome | MONDO_0013362 | |
| glans penis cancer | MONDO_0001388 | |
| penile sarcoma | MONDO_0001387 | |
| visual cortex disorder | MONDO_0003584 | |
| bladder lymphoma | MONDO_0001381 | |
| cortical blindness | MONDO_0001385 | |
| degenerative myopia | MONDO_0001383 | |
| hepatorenal syndrome | MONDO_0001382 | |
| orofacial cleft 10 | MONDO_0013378 | |
| Noonan syndrome 7 | MONDO_0013379 | |
| microphthalmia, isolated, with coloboma 6 | MONDO_0013376 | |
| isolated microphthalmia 7 | MONDO_0013377 | |
| long QT syndrome 6 | MONDO_0013370 |