Additional Disease Briefs

X-linked myotubular myopathy-abnormal genitalia syndrome

Also known as: Xq28 contiguous gene deletion syndrome, myotubular myopathy with abnormal genital development

X-linked neurodegenerative syndrome, Bertini type

X-linked neurodegenerative syndrome, Hamel type

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

X-linked nonsyndromic hearing loss

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

X-linked osteoporosis with fractures

X-linked parkinsonism-spasticity syndrome

Also known as: PARKINSONISM with spasticity, X-linked, Parkinsonism with spasticity, X-linked, X-linked recessive, XPDS

X-linked progressive cerebellar ataxia

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

X-linked recessive ocular albinism

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