All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Pierre Robin syndrome-faciodigital anomaly syndrome | MONDO_0010710 | |
| early-onset parkinsonism-intellectual disability syndrome | MONDO_0010709 | |
| Pallister-W syndrome | MONDO_0010708 | |
| nephropathy - deafness - hyperparathyroidism syndrome | MONDO_0009729 | |
| nephronophthisis 1 | MONDO_0009728 | |
| atelosteogenesis type II | MONDO_0009727 | |
| proteosome-associated autoinflammatory syndrome | MONDO_0009726 | |
| nemaline myopathy 2 | MONDO_0009725 | |
| nail-patella-like renal disease | MONDO_0009724 | |
| obsolete opticoacoustic nerve atrophy with dementia | MONDO_0010701 | |
| optic atrophy--spastic paraplegia syndrome | MONDO_0010700 | |
| Bailey-Bloch congenital myopathy | MONDO_0009722 | |
| ornithine carbamoyltransferase deficiency | MONDO_0010703 | |
| Nathalie syndrome | MONDO_0009721 | |
| orofaciodigital syndrome I | MONDO_0010702 | |
| Keipert syndrome | MONDO_0009720 | |
| obsolete ouabain resistance | MONDO_0010705 | |
| otopalatodigital syndrome type 1 | MONDO_0010704 | |
| Paine syndrome | MONDO_0010707 | |
| reticuloendotheliosis, X-linked | MONDO_0010721 |