spinal cord sarcoma
Also known as: sarcoma of spinal cord, sarcoma of the spinal cord, spinal cord sarcoma
Also known as: sarcoma of spinal cord, sarcoma of the spinal cord, spinal cord sarcoma
Also known as: meningioma (disease) of spinal cord, meningioma of spinal cord, meningioma of the spinal cord, meningioma, spine, spinal cord meningioma, spinal cord meningioma (disease)meningioma (disease) of spinal cord, meningioma of spinal cord, meningioma of the spinal cord, meningioma, spine, spinal cord meningioma, spinal cord meningioma (disease)
Also known as: SMA1 with congenital bone fractures, SMABF1, TRIP4 prenatal-onset spinal muscular atrophy with congenital bone fractures, prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in TRIP4, spinal muscular atrophy type 1 with congenital bone fractures, spinal muscular atrophy with congenital bone fractures 1, spinal muscular atrophy with congenital bone fractures type 1, spinal muscular atrophy, type I, with congenital bone fractures
Also known as: ASCC1 prenatal-onset spinal muscular atrophy with congenital bone fractures, SMABF2, prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in ASCC1, spinal muscular atrophy with congenital bone fractures 2, spinal muscular atrophy with congenital bone fractures type 2
Also known as: SMARD2, X-linked spinal muscular atrophy with respiratory distress, diaphragmatic spinal muscular atrophy type 2, severe infantile axonal neuropathy with respiratory failure type 2
Also known as: Jankovic Rivera syndrome, Jankovic-Rivera syndrome, SMAPME, hereditary myoclonus and progressive distal muscular atrophy, hereditary myoclonus-progressive distal muscular atrophy syndrome, myoclonus hereditary progressive distal muscular atrophy, myoclonus, hereditary, with progressive distal muscular atrophy, spinal muscular atrophy with progressive myoclonic epilepsy
Also known as: SMALED2B, SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT, spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant
Also known as: Dubowitz disease, Intermediate spinal muscular atrophy, SMA II, SMA type 2, SMA type II, SMA-II, SMA2, Sma 2, chronic infantile spinal muscular atrophy, chronic spinal muscular atrophy, muscular atrophy, spinal, Intermediate type, muscular atrophy, spinal, infantile chronic form, muscular atrophy, spinal, intermediate type, proximal spinal muscular atrophy type 2, spinal muscular atrophy type 2, spinal muscular atrophy type II, spinal muscular atrophy, type 2, spinal muscular atrophy, type II, spinal muscular atrophy-2
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