Nervous System Diseases | Page 6

1250 diseases found in 13 pages

H Diseases

Hereditary geniospasm Hereditary hemorrhagic telangiectasia Hereditary hemorrhagic telangiectasia type 2 Hereditary hemorrhagic telangiectasia type 3 Hereditary hemorrhagic telangiectasia type 4 Hereditary hyperekplexia Hereditary motor and sensory neuropathy type 5 Hereditary neuropathy with liability to pressure palsies Hereditary proximal myopathy with early respiratory failure Hereditary sensorimotor neuropathy with hyperelastic skin Hereditary sensory and autonomic neuropathy type 1E Hereditary sensory and autonomic neuropathy type 2 Hereditary sensory and autonomic neuropathy type 7 Hereditary sensory and autonomic neuropathy type V Hereditary sensory neuropathy type 1 Hereditary spastic paraplegia Hereditary vascular retinopathy Hernández-Aguirre Negrete syndrome Herpes simplex encephalitis Herpes zoster oticus HIBCH deficiency Homocystinuria due to CBS deficiency Homocystinuria due to MTHFR deficiency Horizontal gaze palsy with progressive scoliosis Hoyeraal Hreidarsson syndrome HTLV-1 associated myelopathy/tropical spastic paraparesis Human HOXA1 Syndromes Huntington disease Hurler–Scheie syndrome Hurler syndrome Hydranencephaly Hydrocephalus-cleft palate-joint contractures syndrome Hydrocephalus due to congenital stenosis of aqueduct of sylvius Hydroxykynureninuria Hyperbetaalaninemia Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Hyperkalemic periodic paralysis Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency Hyperphenylalaninemia due to dehydratase deficiency Hyperprolinemia Hyperprolinemia type 2 Hypertrophic neuropathy of Dejerine-Sottas Hypocalcemia, autosomal dominant Hypokalemic periodic paralysis Hypomelanosis of Ito Hypomyelination and congenital cataract Hypomyelination with atrophy of basal ganglia and cerebellum Hypoparathyroidism-intellectual disability-dysmorphism syndrome Hypospadias-intellectual disability, Goldblatt type syndrome Hypothalamic hamartomas

I Diseases

Ichthyosis alopecia eclabion ectropion mental retardation Idiopathic intracranial hypertension Idiopathic spinal cord herniation Inclusion body myopathy 2 Inclusion body myopathy 3 Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia Inclusion body myositis Incontinentia pigmenti Infantile axonal neuropathy Infantile cerebellar retinal degeneration Infantile choroidocerebral calcification syndrome Infantile convulsions and paroxysmal choreoathetosis, familial Infantile myofibromatosis Infantile neuroaxonal dystrophy Infantile-onset ascending hereditary spastic paralysis Infantile onset spinocerebellar ataxia Infantile spasms broad thumbs Infection-induced acute encephalopathy 3 Intellectual deficit Buenos-Aires type Intellectual deficit - short stature - hypertelorism Intellectual disability - athetosis - microphthalmia Intellectual disability-developmental delay-contractures syndrome Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity Intellectual disability - hypoplastic corpus callosum - preauricular tag Intellectual disability-severe speech delay-mild dysmorphism syndrome Intellectual disability-spasticity-ectrodactyly syndrome Intermediate congenital nemaline myopathy Internal carotid agenesis Intraneural perineurioma IRVAN syndrome Isaacs' syndrome Isodicentric chromosome 15 syndrome

J Diseases

Johanson-Blizzard syndrome Johnson neuroectodermal syndrome Joubert syndrome Joubert syndrome with oculorenal anomalies Juberg Marsidi syndrome Juvenile amyotrophic lateral sclerosis Juvenile dermatomyositis Juvenile Huntington disease Juvenile polymyositis Juvenile primary lateral sclerosis

K Diseases

Kabuki syndrome Kanzaki disease Kapur Toriello syndrome Kaufman oculocerebrofacial syndrome KBG syndrome KCNQ2-Related Disorders Kearns-Sayre syndrome

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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