Nervous System Diseases | Page 8

1250 diseases found in 13 pages

M Diseases

Megalencephalic leukoencephalopathy with subcortical cysts Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome Megaloblastic anemia due to dihydrofolate reductase deficiency Megalocornea-intellectual disability syndrome Mehes syndrome Meier-Gorlin syndrome Meige syndrome Melnick-Needles syndrome Meningioma Menkes disease Mental retardation skeletal dysplasia abducens palsy Mental retardation Smith Fineman Myers type Mental retardation X-linked syndromic 7 Meralgia paresthetica Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome Methionine adenosyltransferase deficiency Methylcobalamin deficiency cbl G type Methylmalonic acidemia with homocystinuria type cblC MGAT2-CDG (CDG-IIa) Microbrachycephaly ptosis cleft lip Microcephalic osteodysplastic primordial dwarfism type 1 Microcephalic osteodysplastic primordial dwarfism type 2 Microcephalic primordial dwarfism, Montreal type Microcephalic primordial dwarfism Toriello type Microcephaly Microcephaly autosomal dominant Microcephaly brain defect spasticity hypernatremia Microcephaly-cardiomyopathy Microcephaly cervical spine fusion anomalies Microcephaly deafness syndrome Microcephaly glomerulonephritis Marfanoid habitus Microcephaly microcornea syndrome Seemanova type Microcephaly, seizures, and developmental delay Microduplication Xp11.22-p11.23 syndrome Microphthalmia syndromic 10 Microphthalmia syndromic 4 Microphthalmia syndromic 8 Microphthalmia with linear skin defects syndrome Microscopic polyangiitis Micro syndrome Migraine with brainstem aura Mild phenylketonuria Miller-Dieker syndrome Miller-Fisher syndrome Minicore myopathy with external ophthalmoplegia Mitochondrial complex I deficiency Mitochondrial complex II deficiency Mitochondrial DNA-associated Leigh syndrome Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes Mitochondrial Membrane Protein-Associated Neurodegeneration Mitochondrial myopathy and sideroblastic anemia Mitochondrial myopathy with diabetes Mitochondrial myopathy with lactic acidosis Mitochondrial neurogastrointestinal encephalopathy syndrome Mitochondrial trifunctional protein deficiency Mixed connective tissue disease Miyoshi myopathy Moebius syndrome MOGS-CDG (CDG-IIb) Mohr-Tranebjaerg syndrome Molybdenum cofactor deficiency Monoamine oxidase A deficiency Morse-Rawnsley-Sargent syndrome Morvan's fibrillary chorea Mousa Al din Al Nassar syndrome Moyamoya disease MPDU1-CDG (CDG-If) MPI-CDG (CDG-Ib) MPV17-related hepatocerebral mitochondrial DNA depletion syndrome Mucolipidosis type 4 Mucopolysaccharidosis type III Mucopolysaccharidosis type IIIA Mucopolysaccharidosis type IIIB Mucopolysaccharidosis type IIIC Mucopolysaccharidosis type IIID Multiple congenital anomalies-hypotonia-seizures syndrome Multiple congenital anomalies-hypotonia-seizures syndrome type 2 Multiple myeloma Multiple sulfatase deficiency Multiple system atrophy Multisystemic smooth muscle dysfunction syndrome Muscle eye brain disease Muscular dystrophy, congenital, megaconial type Muscular dystrophy white matter spongiosis Muscular phosphorylase kinase deficiency Musculocontractural Ehlers-Danlos syndrome Myasthenia gravis Myelocerebellar disorder Myelomeningocele MYH7-related scapuloperoneal myopathy Myhre syndrome Myoclonic epilepsy with ragged red fibers Myoclonus cerebellar ataxia deafness Myoclonus-dystonia Myoglobinuria recurrent Myopathy with extrapyramidal signs Myosin storage myopathy Myotonia congenita Myotonic dystrophy type 1

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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