All terms in MONDO
| Label | Id | Description |
|---|---|---|
| functional diarrhea | MONDO_0001272 | |
| frontonasal dysplasia with alopecia and genital anomaly | MONDO_0013268 | |
| autosomal recessive nonsyndromic hearing loss 91 | MONDO_0013269 | |
| intellectual disability, autosomal dominant 20 | MONDO_0013266 | |
| distal 16p11.2 microdeletion syndrome | MONDO_0013267 | |
| esophagitis, eosinophilic, 2 | MONDO_0013260 | |
| dilated cardiomyopathy 1R | MONDO_0013261 | |
| amyotrophic lateral sclerosis type 12 | MONDO_0013264 | |
| autism, susceptibility to, 17 | MONDO_0013265 | |
| dilated cardiomyopathy 1S | MONDO_0013262 | |
| retinitis pigmentosa 54 | MONDO_0013263 | |
| obsolete endometriosis of ovary | MONDO_0001289 | |
| osteogenesis imperfecta, type 19 | MONDO_0049223 | |
| endometriosis of rectovaginal septum and vagina | MONDO_0001288 | |
| intellectual disability, X-linked 107 | MONDO_0049222 | |
| endometriosis in cutaneous scar | MONDO_0001287 | |
| myopia 26, X-linked, female-limited | MONDO_0049221 | |
| fallopian tube endometriosis | MONDO_0001282 | |
| alternating exotropia | MONDO_0001281 | |
| endometriosis of pelvic peritoneum | MONDO_0001285 |