All terms in MONDO
| Label | Id | Description |
|---|---|---|
| familial adenomatous polyposis 3 | MONDO_0014630 | |
| classic familial adenomatous polyposis | MONDO_0021055 | |
| DOCK2 deficiency | MONDO_0014637 | |
| combined oxidative phosphorylation defect type 25 | MONDO_0014636 | |
| microphthalmia, isolated, with coloboma 10 | MONDO_0014635 | |
| 46,XY sex reversal 10 | MONDO_0014634 | |
| 46,XY complete gonadal dysgenesis | MONDO_0010765 | |
| mammary Paget disease | MONDO_0002648 | |
| scrotum Paget disease | MONDO_0002649 | |
| scrotal carcinoma | MONDO_0002650 | |
| extramammary Paget disease | MONDO_0008177 | |
| Paget disease of the penis | MONDO_0002653 | |
| autoimmune interstitial lung disease-arthritis syndrome | MONDO_0014629 | |
| basal ganglia calcification, idiopathic, 6 | MONDO_0014628 | |
| dystonia 27 | MONDO_0014627 | |
| scrotum cancer | MONDO_0021112 | |
| hereditary spastic paraplegia 74 | MONDO_0014644 | |
| congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome | MONDO_0014643 | |
| candidiasis, familial, 9 | MONDO_0014642 | |
| chronic mucocutaneous candidiasis | MONDO_0015279 |