neurofibroma, sarcoid, galactosemia, becker muscular dystrophy, degenerative disorder, iritis, autosomal dominant disorder, genetic defect, lichen planus, autosomal recessive disease, dystrophy, chromosomal anomaly, angiosarcoma, superior mesenteric artery, prosopagnosia, retinitis, chromosomal aberration, genetic mutation, polydactylism, myelopathy, genetic abnormality, osteopetrosis, fibroma, photoreceptor, heterotaxy, myotonic dystrophy, roseola, dysgenesis, otosclerosis, cerebri, retinoblastoma, embryonal rhabdomyosarcoma, hyperinsulinism, herpes zoster virus, gene mutation, leukodystrophy, herpesviruses, retinitis pigmentosa, hydrops, opsin, abnormalities, dermoid cyst, synaesthesia, myotonia, hamartoma, xeroderma pigmentosum, severe combined immunodeficiency, monozygotic twin, chlamydial, mosaicism, hypopigmentation, lipoma, genetic disorder, dermatomyositis, leiomyoma, hypertrichosis, plexiform, sensorineural hearing loss, exotropia, blastoma, eccrine, generalized epilepsy, glomerulonephritis, lymphatic tissue, mutation, rh factor, diaphragmatic hernia, entropion, hyperalgesia, ophthalmia, planarian, molluscum, metaplasia, hyperkeratosis, achondroplasia, neurosyphilis, pneumocystis, hydatid disease, aplasia, arthropathy, electrical conduction, trophoblastic, haemolytic anemia, amusia, interstitial pneumonia, bulbar, temporal arteritis, uremia, thyroiditis, photosensitivity, fusiform, myasthenia, pineal, lymphoblastic leukemia, nystagmus, polydactyly, seborrhea, cavefish, myelomeningocele, paresis, nephrosis, histiocytosis, paraplegia, deafness, hemianopia, hemianopsia, amaurosis, aphasia, blindness, hemiplegia, albinism, ataxia, ophthalmoplegia, paralyses, agammaglobulinemia, agenesis, alexia, amblyopia, anosmia, automatism, cataract