M Diseases
From Anvita Health Wiki
Introduction
- maceration
- Machado-Joseph disease
- Machinis syndrome
- Macleod syndrome
- macroamylasemia
- macrocephaly, alopecia, cutis laxa & scoliosis syndrome
- macrocephaly/autism syndrome
- macrocytic anemia
- macrocytosis
- macrophage activation syndrome
- macrothrombocytopenia with sensorineural deafness
- MACS syndrome
- macular amyloidosis
- macular cherry red spot
- macular corneal dystrophy
- macular degeneration
- macular drug red syndrome
- macular dystrophy type 2
- macular edema
- macular hole
- macular pucker
- mad cow disease
- Maffucci's syndrome
- magenblase syndrome
- Majeed syndrome
- major depression
- malabsorption
- malar rash
- malaria
- malaria/HIV coinfection
- malarial hemoglobinuria
- malattia leventinese
- male balding pattern
- male infertility
- male pseudohermaphrodism with gynecomastia
- male pseudohermaphroditism due to 5-alpha-reductase deficiency
- malignancy with infectious etiology
- malignant carcinoid
- malignant ependymoma
- malignant fibrous histiocytoma
- malignant glioma
- malignant histiocytosis
- malignant hypertension
- malignant melanoma
- malignant melanoma of soft parts
- malignant melanoma of the skin
- malignant meningioma
- malignant mesothelioma
- malignant neoplasm
- Malignant Neoplasm (Cancer) Of Ampulla Of Vater
- malignant nerve sheath tumor
- Mallory-Weiss tear
- malnutrition
- malonyl-CoA decarboxylase deficiency
- malposition of the fetus
- MALT lymphoma
- mammal bite
- mammary souffle
- mandibuloacral dysplasia
- mania
- manic depressive psychosis
- mantle cell lymphoma
- map dot fingerprint dystrophy
- maple syrup urine disease
- marasmus
- march hemoglobinuria
- Marchiafava-Bignami disease
- Marchiafava-Micheli syndrome
- Marcus Gunn pupil
- Marfan syndrome
- Marfan syndrome type 2
- Marie Strumpell disease
- Marinesco-Sjoegren syndrome
- Marner type cataract
- Maroteaux-Lamy syndrome
- Marrara
- Martsolf syndrome
- mask of pregnancy
- Mast syndrome
- mastitis
- mastocytoma
- mastocytosis
- mastodynia
- mastoiditis
- Matthew-Wood syndrome
- mature B-cell ALL
- mature onset diabetes of the young
- May-Hegglin anomaly
- Mayer-Rokitansky-Kuster-Hauser syndrome
- McArdle type glycogen storage disease
- McCune-Albright syndrome
- McGrath syndrome
- McLeod syndrome
- Meacham syndrome
- measles
- Meckel syndrome
- Meckel's diverticulum
- medial epicondylitis
- medial otitis
- medial retinaculitis
- median neuropathy
- mediastinal fibrosis
- mediastinal lipomatosis
- mediastinal neoplasm
- mediastinitis
- medication-induced esophagitis
- Mediterranean spotted fever
- medium-chain acyl-CoA dehydrogenase deficiency
- medullary cystic kidney disease
- medullary sponge kidney disease
- medullary thyroid carcinoma
- medulloblastoma
- Mee's lines
- Meesmann corneal dystrophy
- megacolon
- megalencephalic leukoencephalopathy with subcortical cysts
- megaloblastic anemia
- megancephaly
- meibomitis
- Meige lymphedema
- Meige's syndrome
- Meigs' syndrome
- melancholy
- melanocytic nevus
- melanocytoma
- melanodermic leukodystrophy
- melanoma
- melanoma of the skin
- melanoma-astrocytoma syndrome
- melanosis
- MELAS syndrome
- melasma
- Meleda disease
- melena
- melioidosis
- Melkersson-Rosenthal syndrome
- Melnick-Fraser syndrome
- Melnick-Needles syndrome
- membranoproliferative glomerulonephritis
- membranous glomerulonephritis
- memory impairment
- memory impairment in Alzheimer's disease
- Mendelian susceptibility to mycobacterial disease
- Mendelson's syndrome
- Mendenhall syndrome
- Menetrier's disease
- Meniere's disease
- meningeal hemangiopericytoma
- meningeal leukemia
- meningeal neoplasm
- meningioma
- meningitis
- meningococcemia
- meningoencephalitis
- Menkes disease
- menopausal symptom
- menopause
- menorrhagia
- menstrual pain
- mental neuropathy
- mental retardation
- mental retardation syndromic X-linked JARID1C-related
- mental retardation syndromic X-linked Turner type
- mental retardation syndromic X-linked with hypotonic facies syndrome type 1
- mental retardation syndromic X-linked ZDHHC9-related
- mental retardation, nonsyndromic
- mental retardation, nonsyndromic autosomal recessive 2A
- mental retardation, nonsyndromic autosomal recessive 3
- mental retardation, nonsyndromic autosomal recessive 6
- mental retardation-aphasia-shuffling gait-adducted thumbs syndrome
- mental retardation-joint hypermobility-skin laxity
- mental retardation-truncal obesity-retinal dystrophy-micropenis
- meralgia paresthetica
- mercury toxicity
- Meretoja type amyloidosis
- Merkel Cell Carcinoma
- MERRF syndrome
- mesangial proliferative glomerulonephritis
- mesangiocapillary glomerulonephritis
- mesenteric adenitis
- mesenteric ischemia
- mesothelioma
- metabolic acidosis
- metabolic alkalosis
- metabolic syndrome
- metachromatic leukodystrophy
- metachromatic leukodystrophy childhood form
- metachromatic leukodystrophy due to cerebroside sulfatase activator deficiency
- metagonimiasis
- metal fume fever
- metamorphopsia
- metastasis
- metastatic cancer of unknown primary
- metatarsalgia
- methacrylic aciduria
- methanol intoxication
- methemoglobin reductase deficiency
- methemoglobinemia
- methylcobalamin deficiency type E
- methylcobalamin deficiency type G
- methylcrotonoyl-CoA carboxylase deficiency
- methylenetetrahydrofolate reductase deficiency
- methylglutaconic aciduria
- methylglutaconyl-CoA hydratase deficiency
- methylmalonate semialdehyde dehydrogenase deficiency
- methylmalonic acidemia
- methylmalonic aciduria & homocystinuria
- metorchiasis
- mevalonicaciduria
- MGUS
- MI (myocardial infarction)
- microalbuminuria
- microangiopathic hemolytic anemia
- microcephalic osteodysplastic primordial dwarfism
- microcephaly
- microcephaly Amish type
- microcoria-congenital nephrotic syndrome
- microcytic anemia
- microphthalmia
- microphthalmia 3, syndromic
- microphthalmia 5, syndromic
- microphthalmia 7, syndromic
- microphthalmia 8, syndromic
- microphthalmia 9, syndromic
- microphthalmia isolated type 3
- microphthalmia isolated with cataract type 2
- microphthalmia with associated anomalies 2
- microphthalmia with cataracts & iris abnormalities
- microphthalmia with coloboma 3
- microphthalmia with coloboma 5
- microphthalmia, dermal aplasia & sclerocornea [MIDAS] syndrome
- micropolygyria
- micropsia
- microscopic colitis
- microscopic polyangiitis
- microspherocytosis
- microsporidiosis
- microvascular angina
- micturition syncope
- middle ear effusion
- midline granuloma
- midline malignant reticulocytosis
- midsystolic click
- migraine
- migratory arthritis
- migratory necrolytic erythema
- Mikulicz syndrome
- mild-persistent asthma
- miliaria
- miliaria crystallina
- miliaria profunda
- miliaria rubra
- milium
- milk intolerance
- milk-alkali syndrome
- Miller syndrome
- Miller-Dieker lissencephaly syndrome
- Miller-Fisher syndrome
- Milton's disease
- Milwaukee shoulder/knee syndrome
- mineralocorticoid deficiency
- mineralocorticoid excess
- mineralocorticoid receptor activation
- minimal change disease
- minimal cognitive impairment
- minimal trauma fracture
- minimally conscious state
- miosis
- Mirrizi's syndrome
- mirror-image polydactyly of hands & feet without other anomalies
- miscarriage
- mitochondrial acetoacetyl CoA thiolase deficiency
- mitochondrial complex IV deficiency
- mitochondrial DNA depletion syndrome type 3
- Mitochondrial Encephalomyopathy, Lactic Acidosis & Stroke-like episodes
- mitochondrial HSP60 chaperonopathy
- mitochondrial myopathy
- mitochondrial myopathy & sideroblastic anemia
- mitochondrial phosphate carrier deficiency
- mitochondrial sensorineural deafness
- mitral regurgitation
- mitral stenosis
- mitral valve prolapse
- mitral valve replacement
- mittelschmerz
- mixed acid-base disorder
- mixed cell leukemia
- mixed cellular&humoral immune dysfunction
- mixed connective tissue disease
- mixed dementia
- mixed glioma
- mixed hearing loss
- mixed urinary incontinence
- Miyoshi myopathy
- Mobitz type 1 second-degree atrioventricular block
- Mobitz type 2 second-degree atrioventricular block
- Mobius syndrome
- MODY (mature onset diabetes of the young)
- Mohr-Traneberg syndrome
- mole (melanocytic nevus)
- Mollaret's meningitis
- molluscum contagiosum
- molybdenum cofactor deficiency
- Monckenberg's arteriosclerosis
- Mongolian spot
- monilethrix
- moniliasis
- monkeypox
- monoarticular arthritis
- monocarboxylate transporter 8 deficiency
- monoclonal cryoglobulinemia
- monoclonal gammopathy
- monoclonal gammopathy of undetermined significance
- monocyte dysfunction
- monocytopenia
- monocytosis
- monomelic amyotrophy
- monomorphic ventricular tachycardia
- mononeuritis multiplex
- mood disorder
- morbilliform exanthem
- Morfan's syndrome
- Morgellons
- Morgellons disease
- morning sickness
- morning stiffness
- morphea
- Morquio disease
- Morquio disease type-B
- Morrant-Baker cyst
- Morton's foot
- Morton's neuroma
- mosaic variegated aneuploidy syndrome
- motion sickness
- motor neuron disease
- motor vehicle accident
- mottled skin
- mourning
- movement disorder
- movement-related pain
- Mowat-Wilson syndrome
- moyamoya disease
- Moynahan's syndrome
- mu-chain disease
- mucinous adenocarcinoma
- mucinous pancreatic duct ectasia
- Muckle-Wells syndrome
- mucocele
- mucocutaneous candidiasis
- mucocutaneous leishmaniasis
- mucocutaneous lymph node disease
- mucolipidosis
- mucolipidosis 1
- mucopolysaccharidosis 3A
- mucopolysaccharidosis 3B
- mucopolysaccharidosis 3C
- mucopolysaccharidosis 4b
- mucopolysaccharidosis 9
- mucopolysaccharidosis-1 & 5
- mucopolysaccharidosis-2
- mucopolysaccharidosis-3
- mucopolysaccharidosis-4
- mucopolysaccharidosis-6
- mucopolysaccharidosis-7
- mucormycosis
- mucosal erosion
- mucosal ulcer
- mucositis
- mucosulfatidosis
- mucous plugging
- Muehrcke's nails
- Muenke syndrome
- Muir-Torre syndrome
- Mulder's sign
- Mulibrey nanism
- multi-infarct dementia
- multicentric osteolysis nodulosis & arthropathy
- multicentric reticulohistiocytosis
- multifocal atrial tachycardia
- multifocal motor neuropathy
- multiminicore disease with external ophthalmoplegia
- multinodular goiter
- multinodular toxic goiter
- multiple acyl CoA dehydrogenase deficiency
- multiple chemical sensitivity syndrome
- multiple coagulation factor deficiency 1
- multiple cutaneous & uterine leiomyomata
- multiple endocrine neoplasia 4
- multiple endocrine neoplasia type-1
- multiple endocrine neoplasia type-2
- multiple endocrine neoplasia type-2A
- multiple endocrine neoplasia type-2B
- multiple epiphyseal dysplasia
- multiple epiphyseal dysplasia with early-onset diabetes mellitus
- multiple familial trichoepithelioma type 1
- multiple hamartoma syndrome
- multiple hereditary exostosis
- multiple lentigenes syndrome
- multiple mucosal neuromas syndrome
- multiple myeloma
- multiple organ dysfunction syndrome
- multiple personality disorder
- multiple sclerosis
- multiple sulfatase deficiency
- multiple synostoses syndrome
- multiple synostoses syndrome 1
- multiple system atrophy
- multiple system tauopathy with presenile dementia
- mumps
- Munchausen syndrome
- murine typhus
- murmur
- murmur of the heart
- Murphy sign
- muscarine toxicity
- muscle cramp
- muscle eye brain disease
- muscle pain
- muscle rigidity
- muscle spasm
- muscle twitching
- muscle weakness
- muscle-specific enolase-beta deficiency
- muscular disease
- muscular dystrophy
- muscular dystrophy type 1C
- muscular dystrophy type 1D
- muscular hypotonia
- musculoskeletal disease
- musculoskeletal pain
- mutilating keratoderma with ichthyosis
- myalgia
- myalgic encephalomyelitis
- myasthenia angiosclerotic
- myasthenia gravis
- myasthenic syndrome
- mycobacterial infection
- mycobacterial infections in patients with HIV
- mycosis
- mycosis fungoides
- mycotic aneurysm
- MYD88 deficiency
- mydriasis
- myelinoclastic diffuse sclerosis
- myelodysplastic syndrome
- myelofibrosis
- myeloid metaplasia
- myeloid sarcoma
- myelolipoma
- myeloma cast nephropathy
- myeloma kidney
- myelopathy
- myeloperoxidase deficiency
- myelophthisic anemia
- myeloproliferative disorder
- myelosuppression
- Myerson's sign
- myiasis
- myocardial infarction
- myocardial ischemia
- myocarditis
- myoclonic dystonia
- myoclonic encephalopathy of infants
- myoclonic epilepsy associated with ragged-red fibers
- myoclonic epilepsy of Lafora
- myoclonic epilepsy type 1
- myoclonic seizure
- myoclonus
- myoclonus-renal failure syndrome
- myofascial pain
- myofascial pain dysfunction syndrome
- myofascial pain syndrome
- myofibrillar myopathy
- myofibroblastic neoplasm
- myofibromatosis
- myofibrosis
- myoglobinuria
- myokymia
- myopathic mitochondrial DNA depletion syndrome
- myopathy
- myopathy due to phosphoglycerate mutase deficiency
- myopathy SEPN-related
- myopathy with lactic acidosis & sideroblastic anemia
- myopia
- myosin storage myopathy
- myositis
- myositis ossificans
- myotilinopathy
- myotonia
- myotonia congenita
- myotonia fluctuans
- myotonia permanens
- myotonia SCN4A-related
- myotonic dystrophy
- myotonic dystrophy 2
- myringitis
- myxedema
- myxoid cyst
- myxoid liposarcoma
- myxoma
- myxopapillary ependymoma
More General Terms
M - diseases
