Nervous System Diseases | Page 7

1250 diseases found in 13 pages

K Diseases

Kennedy disease Keratosis follicularis dwarfism and cerebral atrophy Kernicterus Keutel syndrome King Denborough syndrome Kleine Levin syndrome Klumpke paralysis Kosztolanyi syndrome Kozlowski-Krajewska syndrome Kuru Kuzniecky Andermann syndrome

L Diseases

L-2-hydroxyglutaric aciduria Laband syndrome La Crosse encephalitis Lafora disease Laing distal myopathy Lambert Eaton myasthenic syndrome Landau-Kleffner syndrome L-arginine:glycine amidinotransferase deficiency Late-onset distal myopathy, Markesbery-Griggs type Lateral meningocele syndrome Laurence-Moon syndrome LCHAD deficiency Leber hereditary optic neuropathy with dystonia Leigh syndrome, French Canadian type Lennox-Gastaut syndrome Lenz Majewski hyperostotic dwarfism Lenz microphthalmia syndrome Lesch Nyhan syndrome Leukodystrophy Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia Leukoencephalopathy - dystonia - motor neuropathy Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Leukoencephalopathy with thalamus and brainstem involvement and high lactate Levic Stefanovic Nikolic syndrome Lewis-Sumner syndrome Lhermitte-Duclos disease Li-Fraumeni syndrome Limb-girdle muscular dystrophy type 1A Limb-girdle muscular dystrophy type 1B Limb-girdle muscular dystrophy type 1C Limb-girdle muscular dystrophy type 1D Limb-girdle muscular dystrophy type 1E Limb-girdle muscular dystrophy type 1F Limb-girdle muscular dystrophy type 1G Limb-girdle muscular dystrophy type 1H Limb-girdle muscular dystrophy type 2A Limb-girdle muscular dystrophy type 2B Limb-girdle muscular dystrophy, type 2C Limb-girdle muscular dystrophy, type 2D Limb-girdle muscular dystrophy type 2E Limb-girdle muscular dystrophy type 2F Limb-girdle muscular dystrophy, type 2G Limb-girdle muscular dystrophy type 2H Limb-girdle muscular dystrophy type 2I Limb-girdle muscular dystrophy type 2J Limb-girdle muscular dystrophy type 2K Limb-girdle muscular dystrophy type 2L Limb-girdle muscular dystrophy type 2M Limb-girdle muscular dystrophy type 2N Limb-girdle muscular dystrophy type 2O Limb-girdle muscular dystrophy type 2P Limb-girdle muscular dystrophy type 2Q Limb-girdle muscular dystrophy type 2S Limb-girdle muscular dystrophy type 2T Limbic encephalitis with LGI1 antibodies Limited cutaneous systemic sclerosis Lipoic acid synthetase deficiency Lissencephaly 1 Lissencephaly 2 Lissencephaly X-linked Localized hypertrophic neuropathy Locked-in syndrome Logopenic progressive aphasia Lowe oculocerebrorenal syndrome Lowry Maclean syndrome Lujan syndrome Lyme disease

M Diseases

Mac Dermot Winter syndrome Macrocephaly-short stature-paraplegia syndrome Macrothrombocytopenia progressive deafness Mal de debarquement syndrome Male pseudohermaphroditism intellectual disability syndrome, Verloes type Malignant hyperthermia Malignant hyperthermia arthrogryposis torticollis Malignant migrating partial seizures of infancy MAN1B1-CDG Mandibulofacial dysostosis with microcephaly Mannosidosis, beta A, lysosomal Marchiafava Bignami disease Marden-Walker syndrome Marfanoid habitus-autosomal recessive intellectual disability syndrome Marinesco-Sjogren syndrome Martsolf syndrome McDonough syndrome McLeod neuroacanthocytosis syndrome Meckel syndrome MECP2 duplication syndrome Medrano Roldan syndrome Medulloblastoma

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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