X-linked non progressive cerebellar ataxia
Also known as: SCAX5, X-linked spinocerebellar ataxia type 5, spinocerebellar ataxia, X-linked 5, spinocerebellar ataxia, X-linked 5, X-linked recessive
Also known as: SCAX5, X-linked spinocerebellar ataxia type 5, spinocerebellar ataxia, X-linked 5, spinocerebellar ataxia, X-linked 5, X-linked recessive
Also known as: X-linked deafness, X-linked isolated neurosensory deafness type DFN, X-linked isolated neurosensory hearing loss type DFN, X-linked isolated sensorineural deafness type DFN, X-linked isolated sensorineural hearing loss type DFN, X-linked non-syndromic neurosensory deafness type DFN, X-linked non-syndromic neurosensory hearing loss type DFN, X-linked non-syndromic sensorineural deafness type DFN, X-linked non-syndromic sensorineural hearing loss type DFN, X-linked nonsyndromic deafness, X-linked nonsyndromic genetic deafness, nonsyndromic deafness, X-linked, nonsyndromic genetic deafness, X-linked
Also known as: PARKINSONISM with spasticity, X-linked, Parkinsonism with spasticity, X-linked, X-linked recessive, XPDS
Also known as: OPCA, X-linked, SCAX1, olivopontocerebellar atrophy, X-linked, spinocerebellar ataxia, X-linked 1, spinocerebellar ataxia, X-linked 1, X-linked recessive, spinocerebellar ataxia, X-linked type 1
Also known as: Nettleship-Falls syndrome, Nettleship-Falls type ocular albinism, OA1, X-linked ocular albinism, XLOA, albinism, ocular, type 1, albinism, ocular, type I, ocular albinism type 1, ocular albinism, Nettleship-Falls type, ocular albinism, type I, Nettleship-Falls type
Also known as: PDR, Partington disease, X-linked cutaneous amyloidosis, XLPDR, amyloidosis, familial cutaneous, familial cutaneous amyloidosis, pigmentary disorder, reticulate, with systemic manifestations, pigmentary disorder, reticulate, with systemic manifestations, X-linked, pigmentary disorder, reticulate, with systemic manifestations, X-linked, X-linked recessive
Also known as: PRD, retinal dysplasia X-linked, retinal dysplasia, primary
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