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Subcategories

This category has only the following subcategory.

S

• Spinal muscular atrophy (1 C, 21 P)

Pages in category "Neurogenetic disorders"

The following 27 pages are in this category, out of 27 total. This list may not reflect recent changes.

A

• Allan–Herndon–Dudley syndrome
• Asperger syndrome
• Athabaskan brainstem dysgenesis syndrome

B

• Beck–Fahrner syndrome
• Biotin-thiamine-responsive basal ganglia disease

C

• Congenital distal spinal muscular atrophy
• Congenital fiber type disproportion

D

• GLUT1 deficiency
• Dejerine–Sottas disease
• Dentatorubral–pallidoluysian atrophy
• Distal spinal muscular atrophy type 1

F

• FBXW7 neurodevelopmental syndrome
• Fragile X syndrome

H

• Hereditary motor and sensory neuropathy
• Hereditary sensory and autonomic neuropathy
• Hereditary sensory and autonomic neuropathy type I

K

• Kohlschütter–Tönz syndrome

M

• Mandibulofacial dysostosis-microcephaly syndrome
• McLeod syndrome

N

• Neotenic complex syndrome

P

• Pontocerebellar hypoplasia

R

• Roussy–Lévy syndrome

S

• Salt and pepper syndrome
• Severe intellectual disability-progressive spastic diplegia syndrome
• SYNGAP1-related intellectual disability

T

• Tourette syndrome
• TRPM3-related neurodevelopmental disorder

• Genetic disorders by system
• Congenital disorders of nervous system