All terms in MONDO
| Label | Id | Description |
|---|---|---|
| glutathione synthetase deficiency with 5-oxoprolinuria | MONDO_0009947 | |
| hemolytic anemia due to pyrimidine 5' nucleotidase deficiency | MONDO_0009946 | |
| pyloric atresia | MONDO_0009944 | |
| nasal dermoid cyst | MONDO_0010921 | |
| facial dermoid cyst | MONDO_0015380 | |
| pyknoachondrogenesis | MONDO_0009942 | |
| proximal myopathy with focal depletion of mitochondria | MONDO_0010923 | |
| Pygmy | MONDO_0009941 | |
| Satoyoshi syndrome | MONDO_0010922 | |
| pycnodysostosis | MONDO_0009940 | |
| velo-facial-skeletal syndrome | MONDO_0010925 | |
| orofacial cleft 3 | MONDO_0010927 | |
| isolated cleft palate | MONDO_0007336 | |
| familial hypocalciuric hypercalcemia 3 | MONDO_0010926 | |
| nocturnal enuresis, 2 | MONDO_0010941 | |
| obsolete short stature-microcephaly-heart defect syndrome | MONDO_0022921 | |
| obsolete daentl towsend Siegel syndrome | MONDO_0022926 | |
| low phospholipid associated cholelithiasis | MONDO_0010939 | |
| peroxisome biogenesis disorder type 3B | MONDO_0009959 | |
| adult Refsum disease | MONDO_0009958 |