All terms in MONDO
| Label | Id | Description |
|---|---|---|
| congenital hypotrichosis milia | MONDO_0022841 | |
| Sillence syndrome | MONDO_0007227 | |
| brachymesomelia-renal syndrome | MONDO_0007228 | |
| autosomal recessive polycystic kidney disease | MONDO_0009889 | |
| congenital mumps | MONDO_0022843 | |
| polycystic kidney, cataract, and congenital blindness | MONDO_0009888 | |
| fibular aplasia-ectrodactyly syndrome | MONDO_0007225 | |
| pseudoaminopterin syndrome | MONDO_0010865 | |
| brachydactyly-nystagmus-cerebellar ataxia syndrome | MONDO_0007226 | |
| desquamative interstitial pneumonia | MONDO_0009887 | |
| rippling muscle disease 1 | MONDO_0010868 | |
| pleoconial myopathy with salt craving | MONDO_0009886 | |
| brachydactyly type E1 | MONDO_0007223 | |
| PARC syndrome | MONDO_0010867 | |
| brachydactyly, type E, with atrial septal defect, type 2 | MONDO_0007224 | |
| Scott syndrome | MONDO_0009885 | |
| platelet prostacyclin receptor defect | MONDO_0009884 | |
| brachydactyly type C | MONDO_0007221 | |
| motor neuron disease with dementia and ophthalmoplegia | MONDO_0010869 | |
| ophthalmoplegia | MONDO_0003425 |