All terms in MONDO
| Label | Id | Description |
|---|---|---|
| 5-oxoprolinase deficiency | MONDO_0009825 | |
| primary hyperoxaluria type 2 | MONDO_0009824 | |
| primary hyperoxaluria type 1 | MONDO_0009823 | |
| Wolfram syndrome, mitochondrial form | MONDO_0010800 | |
| otoonychoperoneal syndrome | MONDO_0009822 | |
| lethal osteosclerotic bone dysplasia | MONDO_0009821 | |
| pancreatic hypoplasia-diabetes-congenital heart disease syndrome | MONDO_0010802 | |
| osteoporosis-pseudoglioma syndrome | MONDO_0009820 | |
| spondylocamptodactyly syndrome | MONDO_0010801 | |
| obsolete BRCATA | MONDO_0010804 | |
| Eiken syndrome | MONDO_0010803 | |
| retinitis pigmentosa 13 | MONDO_0010806 | |
| bladder exstrophy | MONDO_0010805 | |
| MONDO_0022808 | MONDO_0022808 | |
| Colver Steer Godman syndrome | MONDO_0022809 | |
| autosomal recessive juvenile Parkinson disease 2 | MONDO_0010820 | |
| Collins-Sakati syndrome | MONDO_0022802 | |
| coloboma porencephaly hydronephrosis | MONDO_0022803 | |
| colobomata unilobar lung heart defect | MONDO_0022804 | |
| colonic malakoplakia | MONDO_0022805 |