| Label | Id | |
|---|---|---|
| ideomotor apraxia | 6800.0 | |
| chromosome 18p deletion syndrome | 7800.0 | |
| trichoepithelioma, multiple familial, 2 | 12800.0 | |
| Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | 13800.0 | |
| GLM4 | 11800.0 | |
| robinow syndrome, autosomal recessive 2 | 32800.0 | |
| Blount disease, adolescent | 9800.0 | |
| mitochondrial membrane transport disorder | 16800.0 | |
| Wolfram syndrome, mitochondrial form | 10800.0 |