Create issue ticket

219 Possible Causes for Lower Extremity-Predominant Spinal Muscular Atrophy Type 2

  • Autosomal Dominant Spastic Paraplegia Type 9A

    extremity-predominant spinal muscular atrophy type 2 AD 12 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • X-linked Parkinsonism-Spasticity Syndrome

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Autosomal Recessive Spastic Paraplegia Type 63

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Familial Hypercholesterolemia

    Spinal Muscular Atrophy, Lower Extremity-Predominant, 2 4 Spinal Muscular Atrophy, Type I 1 Spinal Muscular Atrophy, Type II 1 Spinal Muscular Atrophy, Type III 1 Spinal[preventiongenetics.com] Muscular Atrophy, Distal, Congenital Nonprogressive 1 Spinal Muscular Atrophy, Distal, X-Linked 3 3 Spinal Muscular Atrophy, Lower Extremity, Autosomal Dominant; SMALED 2[preventiongenetics.com] Myopathy 1 Sphingolipid Activator Protein 1 Deficiency 2 Spinal Muscular Atrophy With Respiratory Distress 1 2 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 5 1 Spinal[preventiongenetics.com]

  • Diomedi-Bernardi-Placidi Syndrome

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Autosomal Recessive Spastic Paraplegia Type 27

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Autosomal Recessive Spastic Paraplegia Type 64

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Autosomal Recessive Spastic Paraplegia Type 44

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

  • Autosomal Recessive Spastic Paraplegia Type 46

    extremity-predominant spinal muscular atrophy type 2 AD 13 BSCL2 606158 Lipodystrophy, congenital generalized, type 2; spastic paraplegia 17; Neuropathy, distal hereditary[centogene.com] […] autosomal dominant; spastic paraplegia 9B; Cutis laxa, autosomal dominant 3 AD, AR 8 ATL1 606439 spastic paraplegia 3A AD 37 ATP2B4 108732 0 BICD2 609797 autosomal dominant lower[centogene.com]

Further symptoms