Simplifying Science™
| A | From AB GM2-gangliosidosis, Type to Azorean neurologic disease |
| B | From bacillus conjunctivitis, Koch-Weeks to bulbospinal neuronopathy, X-linked recessive |
| C | From calcific band keratopathy to cytopathy, mitochondrial |
| D | From dancing eyes-dancing feet syndrome to dystrophy, unspecified, progressive muscular |
| E | From E. coli meningitis to eyes-dancing feet syndrome, dancing |
| F | From FA to furuncle, eyelid |
| G | From galactocerebrosidase deficiency to Guillain-Barre syndrome |
| H | From Haemophilus aegyptius conjunctivitis to HYPP |
| I | From idiopathic intracranial hypertension to IV, OPCA |
| J | From Jansky-Bielschowsky disease to juvenile-onset neuroaxonal dystrophy |
| K | From KD to KWS |
| L | From labyrinthitis to lumbrosacral plexus lesion |
| M | From Machado-Joseph disease to myotubular myopathy, X-linked |
| N | From narcolepsy to NSRD1 |
| O | From OAK to otomycosis |
| P | From pachymeningitis, Haemophilus to pyogenic venous thrombosis |
| Q | From 16q22-linked spinocerebellar ataxia to quadriplegia |
| R | From radicular neuropathy, autosomal dominant hereditary sensory to RSD |
| S | From Sandhoff disease to system, spongy degeneration of central nervous |
| T | From Tay-Sachs disease to typical nemaline myopathy |
| U | From upper motor neuron syndrome to uveoretinitis, idiopathic |
| V | From V hereditary sensory and autonomic neuropathy, Type to Vogt-Spielmeyer disease |
| W | From Wadia-Swami syndrome to wide-angle glaucoma |
| X | From X-linked bulbospinal muscular atrophy to XLMTM |
| Y | Yuge's syndrome |
