List of diseases (M)
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Diseases |
Ma
Mac
pussy dieseas
Maci-Macr
- Macias Flores Garcia Cruz Rivera syndrome
- Mackay Shek Carr syndrome
- Macleod Fraser syndrome
- Macrocephaly cutis marmorata telangiectatica
- Macrocephaly dominant type
- Macrocephaly mental retardation facial dysmorphism
- Macrocephaly mesodermal hamartoma spectrum
- Macrocephaly mesomelic arms talipes
- Macrocephaly pigmentation large hands feet
- Macrocephaly short stature paraplegia
- Macrodactyly of the foot
- Macrodactyly of the hand
- Macroepiphyseal dysplasia Mcalister Coe type
- Macroglobulinemia
- Macroglossia dominant
- Macroglossia exomphalos gigantism
- Macrogyria pseudobulbar palsy
- Macrophagic myofasciitis
- Macrosomia developmental delay dysmorphism
- Macrosomia microphthalmia cleft palate
- Macrothrombocytopenia progressive deafness
- Macrothrombocytopenia with leukocyte inclusions
Macu
- Macular corneal dystrophy
- Macular degeneration juvenile
- Macular degeneration, age-related
- Macular degeneration, polymorphic
- Macular degeneration
- Macular dystrophy, vitelliform
- Macules hereditary congenital hypopigmented and hyperpigmented
Mad-Mag
- Mad cow disease
- Madelung's disease
- Madokoro Ohdo Sonoda syndrome
- Maffucci syndrome
- Maghazaji syndrome
- Magnesium defect in renal tubular transport of
- Magnesium wasting renal
Mal
Mala-Mall
- Malakoplakia
- Malaria
- Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency
- Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency
- Male pseudohermaphroditism due to defective LH molecule
- Malformations in neuronal migration
- Malignant astrocytoma
- Malignant fibrous histiocytoma
- Malignant germ cell tumor
- Malignant hyperthermia arthrogryposis torticollis
- Malignant hyperthermia susceptibility type 1
- Malignant hyperthermia susceptibility type 2
- Malignant hyperthermia susceptibility type 3
- Malignant hyperthermia susceptibility type 4
- Malignant hyperthermia susceptibility type 5
- Malignant hyperthermia susceptibility type 6
- Malignant hyperthermia
- Malignant mesenchymal tumor
- Malignant mixed Mullerian tumor
- Malignant paroxysmal ventricular tachycardia
- Mallory-Weiss syndrome
Malo-Malp
- Malonic aciduria
- Malonyl-CoA decarboxylase deficiency
- Malouf syndrome
- Malpuech facial clefting syndrome
Man
- Mandibuloacral dysplasia
- Mandibulofacial dysostosis deafness postaxial polydactyly
- Manic Depression, Bipolar
- Manic-depressive psychosis, genetic types
- Mannosidosis
- Manouvrier syndrome
- Mansonelliasis
- Mantle cell lymphoma
Mar
Mara-Marg
- Marashi Gorlin syndrome
- Marburg fever
- Marchiafava Bignami disease
- Marchiafava-Micheli disease
- Marcus Gunn phenomenon
- Marden Walker like syndrome
- Marden-Walker syndrome
- Marek disease
- Marfan Syndrome type II
- Marfan Syndrome type III
- Marfan Syndrome type IV
- Marfan Syndrome type V
- Marfan syndrome
- Marfan-like syndrome, Boileau type
- Marfan-Like syndrome
- Marfanoid craniosynostosis syndrome
- Marfanoid hypermobility
- Marfanoid mental retardation syndrome autosomal
- Marginal glioneuronal heterotopia
Mari-Mart
- Marie type ataxia
- Marie Unna congenital hypotrichosis
- Marinesco Sjogren like syndrome
- Marinesco-Sjogren syndrome
- Marion Mayers syndrome
- Markel Vikkula Mulliken syndrome
- Marles Greenberg Persaud syndrome
- Maroteaux Cohen Solal Bonaventure syndrome
- Maroteaux Fonfria syndrome
- Maroteaux Le Merrer Bensahel syndrome
- Maroteaux Stanescu Cousin syndrome
- Maroteaux Verloes Stanescu syndrome
- Maroteaux-Lamy syndrome
- Marphanoid syndrome type De Silva
- Marsden Nyhan Sakati syndrome
- Marsden syndrome
- Marshall syndrome
- Marshall-Smith syndrome
- Martinez Monasterio Pinheiro syndrome
- Martsolf Reed Hunter syndrome
- Martsolf syndrome
Mas-May
- MASA syndrome
- Mass syndrome
- Massa Casaer Ceulemans syndrome
- Mast cell disease
- Mastocytosis, short stature, hearing loss
- Mastocytosis
- Mastoiditis
- Mastroiacovo De Rosa Satta syndrome
- Mastroiacovo Gambi Segni syndrome
- MAT deficiency
- Maternal hyperphenylalaninemia
- Maternally inherited diabetes and deafness
- Mathieu De Broca Bony syndrome
- Matsoukas Liarikos Giannika syndrome
- Matthew-Wood syndrome
- Maturity onset diabetes of the young
- Maumenee syndrome
- Maxillary double lip
- Maxillofacial dysostosis
- Maxillonasal dysplasia, Binder type
- Mayer Rokitanski Kuster syndrome
- May-Hegglin Anomaly
Mc
- McAlister Crane syndrome
- McArdle disease
- McCallum Macadam Johnston syndrome
- McCune-Albright syndrome
- McDonough syndrome
- McDowall syndrome
- McGillivray syndrome
- McKusick Kaufman syndrome
- McKusick type metaphyseal chondrodysplasia
- McLain Debakian syndrome
- McPherson Clemens syndrome
- McPherson Robertson Cammarano syndrome
Me
Mea-Med
- Meacham Winn Culler syndrome
- Meadows syndrome
- Measles
- Meckel like syndrome
- Meckel syndrome
- Medeira Dennis Donnai syndrome
- Median cleft lip corpus callosum lipoma skin polyps
- Median nodule of the upper lip
- Mediastinal endodermal sinus tumors
- Mediterranean fever
- Medium-chain Acyl-CoA dehydrogenase deficiency
- Medrano Roldan syndrome
- Medullary cystic disease
- Medullary thyroid carcinoma
- Medulloblastoma
Meg-Mei
- Megacystis microcolon intestinal hypoperistalsis syndrome
- Megaduodenum
- Megaepiphyseal dwarfism
- Megalencephalic leukodystrophy
- Megalencephaly-cystic leukodystrophy
- Megaloblastic anemia
- Megalocornea mental retardation syndrome
- Megalocytic Interstitial Nephritis
- Mehes syndrome
- Mehta Lewis Patton syndrome
- Meier Blumberg Imahorn syndrome
- Meier Rotschild syndrome
- Meige syndrome
- Meigel disease
- Meinecke Pepper syndrome
- Meinecke syndrome
Mel-Mem
- Melanoma type 1
- Melanoma type 2
- Melanoma, familial
- Melanoma, Malignant
- Melanoma-astrocytoma syndrome
- Melanosis neurocutaneous
- MELAS
- Meleda Disease
- Melhem Fahl syndrome
- Melioidosis
- Melkersson-Rosenthal syndrome
- Melnick-Needles osteodysplasty
- Melnick-Needles syndrome
- Membranoproliferative glomerulonephritis (type II)
Men
Mend-Meno
- Mendelian susceptibility to atypical mycobacteria
- Menetrier's disease
- Mengel Konigsmark syndrome
- Ménière's disease
- Meningeal angiomatosis cleft hypoplastic left heart
- Meningioma 1
- Meningioma
- Meningitis, meningococcal
- Meningitis
- Meningocele
- Meningococcemia
- Meningoencephalocele
- Meningoencephalocele-arthrogryposis-hypoplastic thumb
- Meningomyelocele
Ment
Menta
Mental
Mental d-Mental m
Mental r Mental retardation a-Mental retardation m
- Mental retardation anophthalmia craniosynostosis
- Mental retardation arachnodactyly hypotonia telangiectasia
- Mental retardation athetosis microphthalmia
- Mental retardation blepharophimosis obesity web neck
- Mental retardation Buenos Aires type
- Mental retardation cataracts calcified pinnae myopathy
- Mental retardation coloboma slimness
- Mental retardation contractural arachnodactyly
- Mental retardation dysmorphism hypogonadism diabetes
- Mental retardation epilepsy bulbous nose
- Mental retardation epilepsy
- Mental retardation gynecomastia obesity X linked
- Mental retardation hip luxation G6PD variant
- Mental retardation hypocupremia hypobetalipoproteinemia
- Mental retardation hypotonia skin hyperpigmentation
- Mental retardation macrocephaly coarse facies hypotonia
- Mental retardation microcephaly phalangeal facial
- Mental retardation microcephaly unusual facies
- Mental retardation Mietens Weber type
- Mental retardation multiple nevi
- Mental retardation myopathy short stature endocrine defect
- Mental retardation nasal hypoplasia obesity genital hypoplasia
Mental retardation n-Mental retardation s
- Mental retardation nasal papillomata
- Mental retardation osteosclerosis
- Mental retardation progressive spasticity
- Mental retardation psychosis macroorchidism
- Mental retardation short broad thumbs
- Mental retardation short stature absent phalanges
- Mental retardation short stature Bombay phenotype
- Mental retardation short stature cleft palate unusual facies
- Mental retardation short stature deafness genital
- Mental retardation short stature hand contractures genital anomalies
- Mental retardation short stature heart and skeletal anomalies
- Mental retardation short stature hypertelorism
- Mental retardation short stature microcephaly eye
- Mental retardation short stature ocular and articular anomalies
- Mental retardation short stature scoliosis
- Mental retardation short stature unusual facies
- Mental retardation short stature wedge shaped epiphyses
- Mental retardation skeletal dysplasia abducens palsy
- Mental retardation Smith Fineman Myers type
- Mental retardation spasticity ectrodactyly
Mental retardation u-Mental retardation x
- Mental retardation unusual facies Ampola type
- Mental retardation unusual facies Davis Lafer type
- Mental retardation unusual facies talipes hand anomalies
- Mental retardation unusual facies
- Mental retardation Wolff type
- Mental retardation X linked Atkin type
- Mental retardation X linked borderline Maoa metabolism anomaly
- Mental retardation X linked Brunner type
- Mental retardation X linked dysmorphism
- Mental retardation X linked dystonia dysarthria
- Mental retardation X linked severe Gustavson type
- Mental retardation X linked short stature obesity
- Mental retardation X linked Tranebjaerg type seizures psoriasis
- Mental retardation, unexplained
- Mental retardation, X linked, Marfanoid habitus
- Mental retardation, X linked, nonspecific
- Mental retardation, X-linked 14
- Mental retardation
- Mental retardation-polydactyly-uncombable hair
Mer-Mes
- Mercury poisoning
- Meretoja syndrome
- Merkle tumors
- Merlob Grunebaum Reisner syndrome
- Merlob syndrome
- Mesangial sclerosis, diffuse
- Mesenteric ischemia
- Mesenteric panniculitis
- Mesodermal defects lower type
- Mesomelia synostoses
- Mesomelia
- Mesomelic dwarfism cleft palate camptodactyly
- Mesomelic dwarfism Langer type
- Mesomelic dwarfism Nievergelt type
- Mesomelic dwarfism Reinhardt Pfeiffer type
- Mesomelic dysplasia skin dimples
- Mesomelic dysplasia Thai type
- Mesomelic syndrome Pfeiffer type
- Mesothelioma
Met
Meta
- Metabolic acidosis
- Metabolic disorder
- Metabolic syndrome X
- Metacarpals 4 and 5 fusion
- Metachondromatosis
- Metageria
- Metaphyseal anadysplasia
- Metaphyseal chondrodysplasia Schmid type
- Metaphyseal chondrodysplasia Spahr type
- Metaphyseal chondrodysplasia, others
- Metaphyseal dysostosis mental retardation conductive deafness
- Metaphyseal dysplasia maxillary hypoplasia brachydactyly
- Metaphyseal dysplasia Pyle type
- Metastatic insulinoma
- Metatarsus adductus
- Metatrophic dysplasia
- Metatropic dwarfism
Meth
- Methimazole antenatal infection
- Methionine adenosyl transferase deficiency
- Methyl mercury antenatal infection
- Methylcobalamin deficiency cbl G type
- Methylcobalamin deficiency, cbl E complementation type
- Methylenetetrahydrofolate reductase deficiency
- Methylmalonic acidemia with homocystinuria
- Methylmalonic acidemia
- Methylmalonic aciduria microcephaly cataract
- Methylmalonicacidemia with homocystinuria, cbl D
- Methylmalonicaciduria with homocystinuria, cbl F
- Methylmalonicaciduria, vitamin B12 unresponsive, mut-0
- Methylmalonyl-Coenzyme A mutase deficiency
Mev-Mey
Mi
Mic
Mich-Mick
Micr
Mircre
Micro
Microb
Microc
Microcephalic
- Microcephalic osteodysplastic primordial dwarfism
- Microcephalic primordial dwarfism Toriello type
- Microcephalic primordial dwarfism
Microcephaly Microcephaly a-Microcephaly l
- Microcephaly albinism digital anomalies syndrome
- Microcephaly autosomal dominant
- Microcephaly brachydactyly kyphoscoliosis
- Microcephaly brain defect spasticity hypernatremia
- Microcephaly cardiac defect lung malsegmentation
- Microcephaly cardiomyopathy
- Microcephaly cervical spine fusion anomalies
- Microcephaly chorioretinopathy recessive form
- Microcephaly cleft palate autosomal dominant
- Microcephaly deafness syndrome
- Microcephaly developmental delay pancytopenia
- Microcephaly facial clefting preaxial polydactyly
- Microcephaly glomerulonephritis Marfanoid habitus
- Microcephaly hiatus hernia nephrotic syndrome
- Microcephaly hypergonadotropic hypogonadism short stature
- Microcephaly immunodeficiency lymphoreticuloma
- Microcephaly intracranial calcification
- Microcephaly lymphoedema chorioretinal dysplasia
- Microcephaly lymphoedema syndrome
Microcephaly m-Microcephaly w
- Microcephaly mental retardation retinopathy
- Microcephaly mental retardation spasticity epilepsy
- Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome
- Microcephaly microcornea syndrome Seemanova type
- Microcephaly micropenis convulsions
- Microcephaly microphthalmos blindness
- Microcephaly nonsyndromal
- Microcephaly pontocerebellar hypoplasia dyskinesia
- Microcephaly seizures mental retardation heart disorders
- Microcephaly sparse hair mental retardation seizures
- Microcephaly syndactyly brachymesophalangy
- Microcephaly with chorioretinopathy, autosomal dominant form
- Microcephaly with normal intelligence, immunodeficiency
- Microcephaly with spastic quadriplegia
- Microcephaly, holoprosencephaly, and intrauterine growth retardation
- Microcephaly, primary autosomal recessive
- Microcephaly
Microco
- Microcoria, congenital
- Microcornea corectopia macular hypoplasia
- Microcornea glaucoma absent frontal sinuses
Microd-Microv
- Microdontia hypodontia short stature
- Microencephaly
- Microgastria limb reduction defect
- Microgastria short stature diabetes
- Microinfarct
- Micromelic dwarfism Fryns type
- Micromelic dysplasia dislocation of radius
- Microphtalmos bilateral colobomatous orbital cyst
- Microphthalmia camptodactyly mental retardation
- Microphthalmia cataract
- Microphthalmia diaphragmatic hernia Fallot
- Microphthalmia mental deficiency
- Microphthalmia microtia fetal akinesia
- Microphthalmia, Lentz type
- Microphthalmia
- Microphthalmos, microcornea, and sclerocornea
- Microscopic polyangiitis
- Microsomia hemifacial radial defects
- Microspherophakia metaphyseal dysplasia
- Microsporidiosis
- Microtia, meatal atresia and conductive deafness
- Microvillus inclusion disease
Micu
Mid-Mir
- MIDAS syndrome
- Midline cleft of lower lip
- Midline defects autosomal type
- Midline defects recessive type
- Midline developmental field defects
- Midline field defects
- Midline lethal granuloma
- Mietens syndrome
- Mievis Verellen Dumoulin syndrome
- Migraine
- Mikulicz' Disease
- Mikulicz syndrome
- Miller Fisher syndrome
- Miller-Dieker syndrome
- Milner Khallouf Gibson syndrome
- MILS syndrome
- Minkowski-Chauffard disease
- Minoxidil antenatal infection
- Miosis, congenital
- Mirror hands feet nasal defects
- Mirror polydactyly segmentation and limbs defects
Mis-Mix
- Mitochondrial cytopathy (generic term)
- Mitochondrial diseases of nuclear origin
- Mitochondrial diseases, clinically undefinite
- Mitochondrial Diseases
- Mitochondrial encephalomyopathy aminoacidopathy
- Mitochondrial genetic disorders
- Mitochondrial myopathy lactic acidosis
- Mitochondrial myopathy-encephalopathy-lactic acidosis
- Mitochondrial PEPCK deficiency
- Mitochondrial trifunctional protein deficiency
- Mitral atresia
- Mitral regurgitation deafness skeletal anomalies
- Mitral valve prolapse, familial, autosomal dominant
- Mitral valve prolapse, familial, X linked
- Mitral valve prolapse
- Miura syndrome
- Mixed connective tissue disease
- Mixed Mullerian tumor
- Mixed sclerosing bone dystrophy
Ml-Mn
Mo
Mob-Mom
- Mobius syndrome
- MODY syndrome
- Moebius axonal neuropathy hypogonadism
- Moebius syndrome
- Moerman Van den berghe Fryns syndrome
- Moeschler Clarren syndrome
- Mohr syndrome
- Mohr-Tranebjaerg syndrome
- Mollica Pavone Antener syndrome
- Molluscum contagiosum
- Moloney syndrome
- Molybdenum cofactor deficiency
- MOMO syndrome
Mon-Moo
- Mondini Dysplasia
- Mondor's disease
- Monge's disease
- Monilethrix
- Monoamine oxidase A deficiency
- Monoclonal gammopathy of undetermined significance
- Monodactyly tetramelic
- Mononen Karnes Senac syndrome
- Mononeuritis multiplex
- Monosomy 8q12 21
- Monosomy 8q21 q22
- Monosomy X
- Montefiore syndrome
- Moore Federman syndrome
- Moore Smith Weaver syndrome
Mor-Moy
- Morel's ear
- Moreno Zachai Kaufman syndrome
- Morgani Turner Albright syndrome
- Morhosseini Holmes Walton syndrome
- Morillo Cucci Passarge syndrome
- Morphea Scleroderma
- Morphea, generalized
- Morquio disease, type A
- Morquio disease, type B
- Morquio syndrome
- Morrison Young syndrome
- Morse Rawnsley Sargent syndrome
- Motor neuron disease
- Motor neuro-ophthalmic disorders
- Motor neuropathy peripheral dysautonomia
- Motor neuropathy
- Motor sensory neuropathy type 1 aplasia cutis congenita
- Mounier-Kuhn syndrome
- Mount Reback syndrome
- Mousa Al din Al Nassar syndrome
- Moyamoya disease
Mp-Mt
- MPO deficiency
- MPS III-A
- MPS III-B
- MPS III-C
- MPS III-D
- MPS VI
- MRKH Syndrome (Mullerian Agenesis)
- MSBD syndrome
- MTHFR deficiency
Mu
Muc-Mue
- Mucha-Habermann disease
- Muckle-Wells syndrome
- Mucoepithelial dysplasia
- Mucolipidosis type 1
- Mucolipidosis type 3
- Mucolipidosis type 4
- Mucopolysaccharidosis type 3
- Mucopolysaccharidosis type 4
- Mucopolysaccharidosis type I Hurler syndrome
- Mucopolysaccharidosis type I Hurler/Scheie syndrome
- Mucopolysaccharidosis type I Scheie syndrome
- Mucopolysaccharidosis type II Hunter syndrome- mild form
- Mucopolysaccharidosis type II Hunter syndrome- severe form
- Mucopolysaccharidosis type IV-A Morquio syndrome
- Mucopolysaccharidosis type IV-B
- Mucopolysaccharidosis type V
- Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
- Mucopolysaccharidosis type VII Sly syndrome
- Mucopolysaccharidosis
- Mucosulfatidosis
- Muenke Syndrome
Mul
Muli-Mull
- Mulibrey Nanism syndrome
- Muller Barth Menger syndrome
- Mullerian agenesis
- Mullerian aplasia
- Mullerian derivatives lymphangiectasia polydactyly
- Mullerian derivatives, persistent
- Mullerian duct abnormalities galactosemia
- Mulliez Roux Loterman syndrome
Mult
Multi
Multic-Multin
- Multicentric osteolysis nephropathy
- Multicentric reticulohistiocytosis
- Multifocal heterotopia
- Multifocal motor neuropathy with conduction block
- Multifocal ventricular premature beats
- Multinodular goiter cystic kidney polydactyly
Multip
Multiple a-Multiple p
- Multiple acyl-CoA deficiency
- Multiple carboxylase deficiency, biotin responsive
- Multiple carboxylase deficiency, late onset
- Multiple carboxylase deficiency, propionic acidemia
- Multiple chemical sensitivity
- Multiple congenital anomalies mental retardation, growth failure and cleft lip palate
- Multiple congenital contractures
- Multiple contracture syndrome Finnish type
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia, type 2
- Multiple fibrofolliculoma familial
- Multiple hereditary exostoses
- Multiple joint dislocations metaphyseal dysplasia
- Multiple myeloma
- Multiple organ failure
- Multiple pterygium syndrome lethal type
- Multiple pterygium syndrome
Multiple s-Multiple v
- Multiple sclerosis ichthyosis factor VIII deficiency
- Multiple sclerosis
- Multiple subcutaneous angiolipomas
- Multiple sulfatase deficiency
- Multiple synostoses syndrome 1
- Multiple system atrophy
- Multiple vertebral anomalies unusual facies
Mum-Mut
- Mumps
- Munchausen by proxy syndrome
- Muscle-eye-brain syndrome
- Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus
- Muscular dystrophy congenital infantile cataract hypogonadism
- Muscular dystrophy congenital, merosin negative
- Muscular dystrophy facioscapulohumeral
- Muscular dystrophy Hutterite type
- Muscular dystrophy limb girdle type 2A, Erb type
- Muscular dystrophy limb-girdle autosomal dominant
- Muscular dystrophy limb-girdle type 2B, Myoshi type
- Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency
- Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
- Muscular dystrophy white matter spongiosis
- Muscular dystrophy, congenital, merosin-positive
- Muscular dystrophy, Duchenne and Becker type
- Muscular dystrophy
- Muscular fibrosis multifocal obstructed vessels
- Muscular phosphorylase kinase deficiency
- Mutations in estradiol receptor
My
Mya-Myc
- Myalgia eosinophilia associated with tryptophan
- Myalgic encephalomyelitis
- Myasthenia gravis congenital
- Myasthenia gravis
- Myasthenia, familial
- Mycetoma
- Mycobacterium avium complex infection
- Mycoplasmal pneumonia
- Mycosis fungoides lymphoma
- Mycosis fungoides, familial
- Mycosis fungoides
- Mycositis fungoides
Mye-Myi
- Myelinopathies
- Myelitis
- Myelocerebellar disorder
- Myelodysplasia
- Myelodysplastic syndromes
- Myelofibrosis, idiopathic
- Myelofibrosis
- Myelofibrosis-osteosclerosis
- Myeloid splenomegaly
- Myeloperoxidase deficiency
- Myhre Ruvalcaba Graham syndrome
- Myhre Ruvalcaba Kelley syndrome
- Myhre School syndrome
- Myhre syndrome
- Myiasis
Myo
Myoa-Myon
- Myoadenylate deaminase deficiency
- Myocarditis
- Myocardium disorder
- Myoclonic dystonia
- Myoclonic progressive familial epilepsy
- Myoclonus ataxia
- Myoclonus cerebellar ataxia deafness
- Myoclonus epilepsy partial seizure
- Myoclonus epilepsy
- Myoclonus hereditary progressive distal muscular atrophy
- Myoclonus progressive epilepsy of Unverricht and Lundborg
- Myoclonus with epilepsy with ragged red fibers (mitochondria)
- Myoclonus
- Myofibrillar lysis
- Myofibroblastic tumors
- Myoglobinuria dominant form
- Myoglobinuria recurrent
- Myoglobinuria
- Myoneurogastrointestinal encephalopathy syndrome
Myop
- Myopathy and diabetes mellitus
- Myopathy cataract hypogonadism
- Myopathy congenital multicore with external ophthalmoplegia
- Myopathy growth and mental retardation hypospadias
- Myopathy Hutterite type
- Myopathy mitochondrial cataract
- Myopathy Moebius Robin syndrome
- Myopathy ophthalmoplegia hypoacousia areflexia
- Myopathy tubular aggregates
- Myopathy with lactic acidosis and sideroblastic anemia
- Myopathy with lysis of myofibrils
- Myopathy, centronuclear
- Myopathy, desmin storage
- Myopathy, McArdle type
- Myopathy, myotubular
- Myopathy, X-linked, with excessive autophagy
- Myopathy
- Myophosphorylase deficiency
- Myopia
- Myopia, infantile severe
- Myopia, severe
- Myotubular myopathy
Myos-Myot
- Myositis ossificans post-traumatic
- Myositis ossificans progressiva
- Myositis ossificans
- Myositis, inclusion body
- Myositis
- Myotonia atrophica
- Myotonia mental retardation skeletal anomalies
Myx
- Myxedema
- Myxoid liposarcoma
- Myxoma-spotty pigmentation-endocrine overactivity
- Myxomatous peritonitis
- Myxozoa
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .