Nervous System Diseases | Page 5

1250 diseases found in 13 pages

F Diseases

Familial dysautonomia Familial encephalopathy with neuroserpin inclusion bodies Familial exudative vitreoretinopathy Familial focal epilepsy with variable foci Familial hemiplegic migraine Familial hemophagocytic lymphohistiocytosis Familial porencephaly Familial transthyretin amyloidosis Farber's disease Fatal familial insomnia Fatal infantile encephalomyopathy Fatty acid hydroxylase-associated neurodegeneration FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome Febrile infection-related epilepsy syndrome Feigenbaum Bergeron Richardson syndrome Filippi syndrome Fine-Lubinsky syndrome Fingerprint body myopathy Fitzsimmons-Guilbert syndrome Fitzsimmons Walson Mellor syndrome Floating-Harbor syndrome Flynn Aird syndrome Focal dermal hypoplasia Focal segmental glomerulosclerosis Fountain syndrome FOXG1 syndrome Fragile XE syndrome Fragile X syndrome Friedreich ataxia Frontometaphyseal dysplasia Frontotemporal dementia Fryns syndrome Fucosidosis Fukuyama type muscular dystrophy Fumarase deficiency

G Diseases

Galactosialidosis Galloway-Mowat syndrome Gamma aminobutyric acid transaminase deficiency Gangliocytoma GAPO syndrome Gaucher disease type 1 Gaucher disease type 2 Gaucher disease type 3 Gemignani syndrome Genitopatellar syndrome Genoa syndrome Gerstmann-Straussler-Scheinker disease Gerstmann syndrome Giant axonal neuropathy Gillespie syndrome Gliomatosis cerebri Glucose transporter type 1 deficiency syndrome Glutamine deficiency, congenital Glutaric acidemia type I Glutaric acidemia type II Glutaric acidemia type III Glycogen storage disease type 13 Glycogen storage disease type 2 Glycogen storage disease type 3 Glycogen storage disease type 4 Glycogen storage disease type 5 Glycogen storage disease type 7 GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM3 synthase deficiency GMS syndrome Goldberg-Shprintzen megacolon syndrome Gomez Lopez Hernandez syndrome GOSR2-related progressive myoclonus ataxia Graham-Cox syndrome Granulomatosis with polyangiitis Griscelli syndrome type 1 Grubben de Cock Borghgraef syndrome GTPCH1-deficient DRD GTP cyclohydrolase I deficiency Guanidinoacetate methyltransferase deficiency Guillain-Barre syndrome Gurrieri syndrome Gyrate atrophy of choroid and retina

H Diseases

Hair defect-photosensitivity-intellectual disability syndrome Hallermann-Streiff syndrome Hall-Riggs syndrome Hamanishi Ueba Tsuji syndrome Hansen's disease Harding ataxia Harlequin syndrome Harrod Doman Keele syndrome Hartnup disease Hashimoto encephalopathy Hemangioblastoma Hemicrania continua Hemimegalencephaly Hemiplegic migraine Hennekam syndrome Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome Hereditary coproporphyria Hereditary diffuse leukoencephalopathy with spheroids Hereditary endotheliopathy, retinopathy, nephropathy, and stroke Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis

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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