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Rare Diseases Awareness Ribbons - M | Personalized Cause

Blue Jeans awareness ribbons and Zebra awareness ribbons for rare diseases that begin with the letter M. Source of rare diseases: Global Genes®.

RARE DISEASES AND DISORDERS - M

Blue Jeans Awareness Ribbon for Rare Diseases as Designated by Global Genes®

Our Custom Blue Jeans awareness ribbons and non-personalized Blue Jeans awareness ribbons support this list of Rare Diseases as designated by Global Genes®. This list is extensive to include often under-funded, unknown diseases and disorders that need equal attention to those that receive a great deal of funding and recognition. Sometimes you will see a Rare Disease listed in two places on our website, and one may be associated with a color other than the Blue Jeans awareness ribbon. This is because often times a group has designated a color for a Rare Disease prior to the Blue Jeans awareness ribbon being designated for the entire category of causes.

Zebra Awareness Ribbons for Rare Diseases

Our custom zebra awareness ribbons and non-personalized zebra awareness ribbons also support our list of Rare Diseases. As you see on our site, rare diseases also use the blue denim ribbon. Prior to the use of blue jeans awareness ribbons, zebra awareness ribbons represented rare diseases. Rare diseases use a zebra stripe awareness ribbon because of the medical expression “When you hear hoof beats, think horses not zebras” in looking for a common diagnosis versus a rare one.

Our Rare Diseases and Disorders list is extensive to include often under-funded, unknown diseases and disorders that need equal attention to those that receive a great deal of funding and recognition. Sometimes you will see a Rare Disease listed in several places on our website, and one may be associated with a color other than the Blue Jeans awareness ribbon or the zebra awareness ribbon. This is because often times a group has designated a color for a Rare Disease itself rather than the entire category. Feel free to use the image or color that best reflects your efforts to raise awareness.

Mac Dermot Winter syndrome
Macrocephaly mesodermal hamartoma spectrum
Macrocephaly benign familial
Macrocephaly mental retardation short stature spastic paraplegia and CNS malformations
Macrocephaly-capillary malformation
Macrodactyly of the foot
Macrodactyly of the hand
Macroepiphyseal dysplasia with osteoporosis wrinkled skin and aged appearance
Macroglossia
Macrogyria pseudobulbar palsy and mental retardation
Macrophagic myofasciitis
Macrosomia with lethal microphthalmia
Macrothrombocytopenia progressive deafness
Macular dystrophy atypical vitelliform
Macular dystrophy concentric annular
Macular dystrophy corneal type 1
Macules hereditary congenital hypopigmented and hyperpigmented
Madelung disease
Madokoro Ohdo Sonoda syndrome
Maffucci syndrome
Mahvash disease
Majeed syndrome
Mal de debarquement
Malakoplakia
Malaria
Male pseudohermaphroditism due to defective LH molecule
Male pseudohermaphroditism/mental retardation syndrome Verloes type
Malignant cylindroma
Malignant eccrine spiradenoma
Malignant fibrous histiocytoma
Malignant germ cell tumor
Malignant hyperthermia
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 melanoma childhood
Malignant mesenchymal tumor
Malignant mesothelioma
Malignant mixed Mullerian tumor
Malignant paroxysmal ventricular tachycardia
Malignant Teratocarcinosarcoma
Mallory-Weiss syndrome
Malonyl-CoA decarboxylase deficiency
Malouf syndrome
Malpuech facial clefting syndrome
Mandibuloacral dysplasia with type A lipodystrophy
Mandibuloacral dysplasia with type B lipodystrophy
Mandibulofacial dysostosis Treacher Collins type autosomal recessive
Mannosidosis beta A lysosomal
Manouvrier syndrome
Mansonelliasis
Mantle cell lymphoma
Manz syndrome
Maple syrup urine disease
Maple syrup urine disease type 1A
Maple syrup urine disease type 1B
Maple syrup urine disease type 2
Marburg hemorrhagic fever
Marchiafava Bignami disease
Marcus Gunn phenomenon
Marden Walker like syndrome
Marden-Walker syndrome
Marek disease
Marfan syndrome
Marfan Syndrome type 2
Marfan Syndrome type 3
Marfan Syndrome type 4
Marfan Syndrome type 5
Marfanoid hypermobility syndrome
Marfanoid mental retardation syndrome autosomal
Marginal glioneuronal heterotopia
Marie type ataxia
Marie Unna congenital hypotrichosis
Marinesco-Sjogren syndrome
Marinesco-Sjogren-like syndrome (MSLS)
Markel Vikkula Mulliken syndrome
Marles Greenberg Persaud syndrome
Maroteaux Fonfria syndrome
Maroteaux Stanescu Cousin syndrome
Maroteaux Verloes Stanescu syndrome
Marphanoid syndrome type De Silva
Marsden Nyhan Sakati syndrome
Marshall syndrome
Marshall-Smith syndrome
Martinez Monasterio Pinheiro syndrome
Martsolf syndrome
MASS syndrome
Massa Casaer Ceulemans syndrome
Mastocytic enterocolitis
Mastocytosis
Mastocytosis cutaneous with short stature conductive hearing loss and microtia
Mastroiacovo De Rosa Satta syndrome
Mastroiacovo Gambi Segni syndrome
Maternal hyperphenylalaninemia
Maternally inherited Leigh syndrome
Mathieu De Broca Bony syndrome
Matsoukas Liarikos Giannika syndrome
Maturity-onset diabetes of the young
Maturity-onset diabetes of the young type 1
Maturity-onset diabetes of the young type 2
Maturity-onset diabetes of the young type 3
Maturity-onset diabetes of the young type 4
Maturity-onset diabetes of the young type 5
Maturity-onset diabetes of the young type 6
Maturity-onset diabetes of the young type 7
Maturity-onset diabetes of the young type 8
Maturity-onset diabetes of the young type 9
Maumenee syndrome
Maxillary double lip
Maxillofacial dysostosis
Maxillonasal dysplasia Binder type
Mayer-Rokitansky-Kuster-Hauser syndrome
McAlister Crane syndrome
McCallum Macadam Johnston syndrome
McCune Albright syndrome
McDonough syndrome
McDowall syndrome
McGillivray syndrome
McKusick Kaufman syndrome
McLeod neuroacanthocytosis syndrome
McPherson Clemens syndrome
McPherson Robertson Cammarano syndrome
Meacham Winn Culler syndrome
Meadows syndrome
Measles
Meckel syndrome type 2
Meckel syndrome type 3
Meckel syndrome type 1
Meconium aspiration syndrome
Medeira Dennis Donnai syndrome
Medial Medullary Syndrome
Median cleft of upper lip with polyps of facial skin and nasal mucosa
Median nodule of the upper lip
Mediastinal endodermal sinus tumors
Medium-chain 3-ketoacyl-coa thiolase deficiency
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Medrano Roldan syndrome
Medullary cystic kidney disease
Medullary cystic kidney disease 1
Medullary cystic kidney disease 2
Medullary sponge kidney
Medulloblastoma
Medulloblastoma childhood
Meesmann corneal dystrophy
Megacystis microcolon intestinal hypoperistalsis syndrome
Megaduodenum and/or megacystis
Megaepiphyseal dwarfism
Megalencephalic leukoencephalopathy with subcortical cysts
Megalencephaly polymicrogyria and hydrocephalus (MPPH) syndrome
Megalocornea mental retardation syndrome
Megalocytic interstitial nephritis
Megarbane Jalkh syndrome
Megarbane syndrome
Mehes syndrome
Mehta Lewis Patton syndrome
Meier Blumberg Imahorn syndrome
Meier-Gorlin syndrome
Meige syndrome
Meigel disease
Meinecke syndrome
Melanocytic lesions of CNS
Melanoma astrocytoma syndrome
Melanoma familial
Meleda disease
Melhem Fahl syndrome
Meliodosis
Melkersson-Rosenthal syndrome
Melnick-Needles syndrome
Melorheostosis
Membranoproliferative glomerulonephritis type 2
Membranous nephropathy
Menetrier disease
Mengel Konigsmark syndrome
Meningioma
Meningioma spinal
Meningocele
Meningococcal infection
Meningococcemia
Meningoencephalocele
Menkes disease
Mental deficiency-epilepsy-endocrine disorders
Mental retardation anophthalmia craniosynostosis
Mental retardation arachnodactyly hypotonia telangiectasia
Mental retardation athetosis microphthalmia
Mental retardation blepharophimosis obesity web neck
Mental retardation cataracts calcified pinnae myopathy
Mental retardation coloboma slimness
Mental retardation dysmorphism hypogonadism diabetes
Mental retardation epilepsy
Mental retardation epilepsy bulbous nose
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 progressive spasticity
Mental retardation psychosis macroorchidism
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 skeletal dysplasia abducens palsy
Mental retardation Smith Fineman Myers type
Mental retardation spasticity ectrodactyly
Mental retardation syndrome Belgian type
Mental retardation unusual facies
Mental retardation unusual facies talipes hand anomalies
Mental retardation Wolff 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 short stature obesity
Mental retardation X-linked syndromic 11
Mental retardation X-linked syndromic 7
Mental retardation x-linked with cerebellar hypoplasia and distinctive facial appearance
Mental retardation X-linked South African type
Mental retardation epileptic seizures hypogonadism and hypogenitalism microcephaly and obesity
Mental retardation keratoconus febrile seizures and sinoatrial block
Mental retardation macrocephaly short stature and craniofacial dysmorphism
Mental retardation X-linked 14
Mental retardation X-linked nonspecific
Mental retardation-hypotonic facies syndrome X-linked 1
Mental retardation-polydactyly-uncombable hair
Meralgia paresthetica
Mercury poisoning
Meretoja syndrome
Merkel cell carcinoma
Merlob Grunebaum Reisner syndrome
Merlob syndrome
Mesangial proliferative glomerulonephritis
Mesangial sclerosis diffuse
Mesenteric artery ischemia
Mesomelia
Mesomelia-synostoses syndrome
Mesomelic dwarfism cleft palate camptodactyly
Mesomelic dwarfism of hypoplastic tibia and radius type
Mesomelic dysplasia Kantaputra type
Mesomelic dysplasia Savarirayan type
Mesomelic dysplasia skin dimples
Mesomelic syndrome Pfeiffer type
Metacarpals 4 and 5 fusion
Metachondromatosis
Metachromatic leukodystrophy MLD
Metachromatic leukodystrophy due to saposin B deficiency
Metagonimiasis
Metaphyseal acroscyphodysplasia
Metaphyseal anadysplasia
Metaphyseal chondrodysplasia Schmid type
Metaphyseal chondrodysplasia Spahr type
Metaphyseal chondrodysplasia with cone-shaped epiphyses normal hair and normal hands
Metaphyseal chondrodysplasia others
Metaphyseal dysostosis mental retardation conductive deafness
Metaphyseal dysplasia maxillary hypoplasia brachydactyly
Metaphyseal dysplasia without hypotrichosis
Metaphyseal undermodeling spondylar dysplasia and overgrowth
Metaplastic carcinoma of the breast
Metastatic insulinoma
Metastatic squamous neck cancer with occult primary
Metatropic dwarfism
Methimazole antenatal infection
Methionine adenosyltransferase deficiency
Methyl mercury antenatal infection
Methylcobalamin deficiency cbl G type
Methylcobalamin deficiency cbl E complementation type
Methylmalonic acidemia
Methylmalonic acidemia with homocystinuria
Methylmalonic aciduria cblA type
Methylmalonic aciduria cblB type
Methylmalonic aciduria microcephaly cataract
Methylmalonicacidemia with homocystinuria cbl d
Methylmalonicaciduria with homocystinuria cbl f
Methylmalonyl-Coenzyme A mutase deficiency
Mevalonic aciduria
MHC class 1 deficiency
Michelin tire baby syndrome
Michels Caskey syndrome
Michels syndrome
Mickleson syndrome
Micrencephaly corpus callosum agenesis
Microbrachycephaly ptosis cleft lip
Microcephalic osteodysplastic primordial dwarfism type 1
Microcephalic osteodysplastic primordial dwarfism type 2
Microcephalic osteodysplastic primordial dwarfism type 3
Microcephalic osteodysplastic primordial dwarfism with tooth abnormalities
Microcephalic primordial dwarfism Toriello type
Microcephaly
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 deafness syndrome
Microcephaly developmental delay pancytopenia
Microcephaly glomerulonephritis Marfanoid habitus
Microcephaly hypergonadotropic hypogonadism short stature
Microcephaly immunodeficiency lymphoreticuloma
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 with chorioretinopathy autosomal dominant form
Microcephaly with normal intelligence immunodeficiency
Microcephaly with spastic quadriplegia
Microcephaly corpus callosum dysgenesis and cleft lip-palate
Microcephaly hiatal hernia and nephrotic syndrome
Microcephaly holoprosencephaly and intrauterine growth retardation
Microcephaly primary autosomal recessive
Microcoria congenital
Microcornea corectopia macular hypoplasia
Microcornea glaucoma and absent frontal sinuses
Microcystic adnexal carcinoma
Microdeletion 15q11.2
Microdontia hypodontia short stature
Microencephaly
Microgastria limb reduction defect
Microhydranencephaly
Micromelic bone dysplasia with cloverleaf skull
Microphthalmia associated with colobomatous cyst
Microphthalmia camptodactyly mental retardation
Microphthalmia cataract
Microphthalmia diaphragmatic hernia Fallot
Microphthalmia mental deficiency
Microphthalmia microtia fetal akinesia
Microphthalmia syndromic 10
Microphthalmia syndromic 3
Microphthalmia syndromic 4
Microphthalmia syndromic 5
Microphthalmia syndromic 6
Microphthalmia syndromic 7
Microphthalmia syndromic 8
Microphthalmia syndromic 9
Microphthalmia isolated with corectopia
Microscopic polyangiitis
Microsomia hemifacial radial defects
Microspherophakia with hernia
Microsporidiosis
Microtia eye coloboma and imperforation of the nasolacrimal duct
Microtia meatal atresia and conductive deafness
Microtia-Anotia
Microvillus inclusion disease
Midline cleft of lower lip
Midline developmental field defects
Midline field defects
Midline lethal granuloma
Midphalangeal hair
Mikulicz disease
Miles-Carpenter x-linked mental retardation syndrome
Miller Fisher syndrome
Miller-Dieker syndrome
Milner Khallouf Gibson syndrome
Milroy disease
Minicore myopathy with external ophthalmoplegia
Minicore myopathy antenatal onset with arthrogryposis
Minimal change disease
Mirizzi syndrome
Mirror polydactyly segmentation and limbs defects
Mitochondrial complex I deficiency
Mitochondrial complex II deficiency
Mitochondrial complex III deficiency
Mitochondrial complex IV deficiency
Mitochondrial complex V deficiency
Mitochondrial disease with severe hypotonia lactic acidaemia and hyperammonemia
Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
Mitochondrial genetic disorders
Mitochondrial myopathy with diabetes
Mitochondrial myopathy with lactic acidosis
Mitochondrial neurogastrointestinal encephalopathy syndrome
Mitochondrial trifunctional protein deficiency
Mitral atresia
Mitral regurgitation deafness skeletal anomalies
Mitral valve prolapse familial autosomal dominant
Mitral valve prolapse familial X-linked
Miura syndrome
Mixed connective tissue disease
Mixed sclerosing bone dystrophy
Miyoshi myopathy
Moebius axonal neuropathy hypogonadism
Moebius syndrome
Mohr-Tranebjaerg syndrome
Moloney syndrome
Molybdenum cofactor deficiency
MOMO syndrome
Mondini Dysplasia
Mondor's disease
Monilethrix
Monkeypox
Monoamine oxidase A deficiency
Monoclonal gammopathy of undetermined significance
Monodactyly tetramelic
Monomelic amyotrophy
Mononeuritis multiplex
Montefiore syndrome
Morel's ear
Morgagni-Stewart-Morel syndrome
Morgellons
Morillo-Cucci Passarge syndrome
MORM syndrome
Morphea
Morquio syndrome A
Morquio syndrome B
Morquio syndrome C
Morse Rawnsley Sargent syndrome
Morvan's fibrillary chorea
Mosaic trisomy 8
Mosaic trisomy 9
Mosaic variegated aneuploidy syndrome
Motor neuro-ophthalmic disorders
Motor neuropathy peripheral with dysautonomia
Motor sensory neuropathy type 1 aplasia cutis congenita
Mounier-Kuhn syndrome
Mousa Al din Al Nassar syndrome
Mowat-Wilson syndrome
Moyamoya disease
MSBD syndrome
Muckle-Wells syndrome
Mucoepidermoid carcinoma
Mucolipidosis type 3A
Mucolipidosis type 4
Mucopolysaccharidosis
Mucopolysaccharidosis type I
Mucopolysaccharidosis type II
Mucopolysaccharidosis type III
Mucopolysaccharidosis type IIIA
Mucopolysaccharidosis type IIIB
Mucopolysaccharidosis type IIIC
Mucopolysaccharidosis type IIID
Mucopolysaccharidosis type VI
Mucopolysaccharidosis type VII
Muenke Syndrome
Muir-Torre syndrome
Mulibrey Nanism
Muller Barth Menger syndrome
Mullerian agenesis
Mullerian aplasia
Mullerian derivatives persistent
Mullerian duct abnormalities galactosemia
Mulliez Roux Loterman syndrome
Multicentric Castleman’s Disease
Multicentric osteolysis nephropathy
Multicentric reticulohistiocytosis
Multicore disease
Multicystic renal dysplasia bilateral
Multifocal choroiditis
Multifocal fibrosclerosis
Multifocal heterotopia
Multifocal lymphangioendotheliomatosis with thrombocytopenia
Multifocal motor neuropathy with conduction block
Multifocal ventricular premature beats
Multinodular goiter cystic kidney polydactyly
Multiple carboxylase deficiency biotin responsive
Multiple carboxylase deficiency late onset
Multiple carboxylase deficiency propionic acidemia
Multiple congenital anomalies mental retardation growth failure and cleft lip palate
Multiple congenital contractures
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 1
Multiple epiphyseal dysplasia 2
Multiple epiphyseal dysplasia 3
Multiple epiphyseal dysplasia 4
Multiple epiphyseal dysplasia 5
Multiple fibrofolliculoma familial
Multiple joint dislocations metaphyseal dysplasia
Multiple myeloma
Multiple pterygium syndrome Aslan type
Multiple pterygium syndrome Escobar type
Multiple pterygium syndrome lethal type
Multiple pterygium syndrome X-linked
Multiple respiratory chain enzyme deficiencies
Multiple self healing squamous epithelioma
Multiple sulfatase deficiency
Multiple synostoses syndrome 1
Multiple synostoses syndrome 2
Multiple system atrophy
Multiple system atrophy (MSA) with orthostatic hypotension
Multiple vertebral anomalies unusual facies
Munchausen by proxy syndrome
Mungan syndrome
MURCS association
Muscle eye brain disease
Muscular atrophy ataxia retinitis pigmentosa and diabetes mellitus
Muscular dystrophy
Muscular Dystrophy - Late Onset
Muscular dystrophy congenital merosin negative
Muscular dystrophy limb girdle type 2A Erb type
Muscular dystrophy white matter spongiosis
Muscular dystrophy congenital infantile with cataract and hypogonadism
Muscular dystrophy congenital megaconial type
Muscular dystrophy congenital merosin-positive
Muscular fibrosis multifocal obstructed vessels
Muscular phosphorylase kinase deficiency
Mutagen sensitivity
Mutiple parosteal osteochondromatous proliferations
Myalgia eosinophilia associated with tryptophan
Myasthenia gravis
Myasthenia gravis congenital
Myasthenia familial
Myasthenia familial limb-girdle
Myasthenic syndrome congenital associated with acetylcholine receptor deficiency
Myasthenic syndrome congenital slow-channel
Mycetoma
Mycobacterium Abscessus
Mycobacterium Avium Complex
Mycobacterium Chelonae
Mycobacterium fortuitum
Mycobacterium Gordonae
Mycobacterium Kansasii
Mycobacterium Malmoense
Mycobacterium Marinum
Mycobacterium tuberculosis susceptibility to infection by
Mycobacterium Xenopi
Mycoplasmal pneumonia
Mycosis fungoides
Myelitis
Myelocerebellar disorder
Myelocytic leukemia-like syndrome familial chronic
Myelodysplastic syndromes
Myelodysplastic/myeloproliferative disease
Myelofibrosis
Myeloid sarcoma
Myeloid splenomegaly
Myelomeningocele
Myeloperoxidase deficiency
MYH-associated polyposis
MYH9 related thrombocytopenia
Myhre Ruvalcaba Graham syndrome
Myhre Ruvalcaba Kelley syndrome
Myhre School syndrome
Myocarditis
Myoclonus ataxia
Myoclonus cerebellar ataxia deafness
Myoclonus epilepsy
Myoclonus epilepsy partial seizure
Myoclonus hereditary progressive distal muscular atrophy
Myoclonus with epilepsy with ragged red fibers
Myoepithelial carcinoma
Myofibrillar lysis
Myofibrillar myopathy
Myoglobinuria dominant form
Myoglobinuria recurrent
Myokymia with neonatal epilepsy
Myopathic carnitine deficiency
Myopathy cataract hypogonadism
Myopathy congenital
Myopathy congenital multicore with external ophthalmoplegia
Myopathy growth and mental retardation hypospadias
Myopathy mitochondrial cataract
Myopathy ophthalmoplegia hypoacousia areflexia
Myopathy with lysis of myofibrils
Myopathy limb-girdle with bone fragility
Myopathy mitochondrial progressive with congenital cataract hearing loss and developmental delay
Myopathy tubular aggregate
Myopathy X-linked with excessive autophagy
Myopia 6
Myostatin-related muscle hypertrophy
Myotonia atrophica
Myotonia congenita autosomal dominant
Myotonia congenita autosomal recessive
Myotonia mental retardation skeletal anomalies
Myotonic dystrophy
Myotonic dystrophy type 1
Myotonic dystrophy type 2
Myotubular myopathy
Myxoid liposarcoma
Myxoma-spotty pigmentation-endocrine overactivity
Myxomatous peritonitis
Myxopapillary ependymoma
Myxozoa

Source: globalgenes.org
Source: https://rarediseases.info.nih.gov/