All terms in MONDO
| Label | Id | Description |
|---|---|---|
| hereditary sensory and autonomic neuropathy with spastic paraplegia | MONDO_0009748 | |
| Navajo neurohepatopathy | MONDO_0009747 | |
| hereditary sensory and autonomic neuropathy type 4 | MONDO_0009746 | |
| cerebral palsy spastic monoplegic | MONDO_0022700 | |
| spastic monoplegia | MONDO_0001169 | |
| retinitis pigmentosa 2 | MONDO_0010723 | |
| neuronal ceroid lipofuscinosis 5 | MONDO_0009745 | |
| X-linked retinal dysplasia | MONDO_0010722 | |
| neuronal ceroid lipofuscinosis 1 | MONDO_0009744 | |
| X-linked retinoschisis | MONDO_0010725 | |
| neurologic disease, infantile multisystem, with osseous fragility | MONDO_0009743 | |
| obsolete RP6 | MONDO_0010724 | |
| neuroectodermal melanolysosomal disease | MONDO_0009742 | |
| Russell-silver syndrome, X-linked | MONDO_0010727 | |
| neuroblastoma, susceptibility to, 1 | MONDO_0009741 | |
| Rett syndrome | MONDO_0010726 | |
| neurofaciodigitorenal syndrome | MONDO_0009740 | |
| X-linked intellectual disability, Schimke type | MONDO_0010729 | |
| SCARF syndrome | MONDO_0010728 | |
| tooth agenesis, selective, X-linked, 1 | MONDO_0010741 |