|
-
2M3HBA see 17β-hydroxysteroid dehydrogenase type 10 deficiency
-
3-M syndrome
-
3MCC see 3-methylcrotonyl-CoA carboxylase deficiency
-
3MGA see 3-methylglutaconic aciduria
-
M/SCHAD deficiency see 3-hydroxyacyl-CoA dehydrogenase deficiency
-
M3 ANLL see acute promyelocytic leukemia
-
MAA see Lenz microphthalmia syndrome
-
Machado-Joseph disease see spinocerebellar ataxia type 3
- Macular Degeneration see age-related macular degeneration; Stargardt macular degeneration
-
macular degeneration, age-related see age-related macular degeneration
-
macular dystrophy with flecks, type 1 see Stargardt macular degeneration
-
MAD see glutaric acidemia type II
-
MAD deficiency see adenosine monophosphate deaminase deficiency
-
MADA deficiency see adenosine monophosphate deaminase deficiency
-
Maeda syndrome see cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
-
Maffucci syndrome
-
Majeed syndrome
-
Majewski osteodysplastic primordial dwarfism type II see microcephalic osteodysplastic primordial dwarfism type II
-
Malabsorption Syndromes
-
Male Breast Cancer see breast cancer
-
male hypergonadotropic hypogonadism due to LHCGR defect see Leydig cell hypoplasia
-
Male Infertility
-
Male Pattern Alopecia see androgenetic alopecia
-
Male Pattern Baldness see androgenetic alopecia
-
male pseudohermaphroditism due to 5-alpha-reductase deficiency see 5-alpha reductase deficiency
-
Male Turner Syndrome see Noonan syndrome
-
Malherbe calcifying epithelioma see pilomatricoma
-
malignant hyperthermia
-
Malignant neoplasm of breast see breast cancer
-
malignant tumor of breast see breast cancer
-
Malignant tumor of urinary bladder see bladder cancer
-
malonic aciduria see malonyl-CoA decarboxylase deficiency
-
malonyl-CoA decarboxylase deficiency
-
malonyl-coenzyme A decarboxylase deficiency see malonyl-CoA decarboxylase deficiency
-
Mammary cancer see breast cancer
-
mandibulofacial dysostosis (MFD1) see Treacher Collins syndrome
-
Manitoba oculotrichoanal syndrome
-
mannose-binding lectin deficiency
-
mannosidosis see alpha-mannosidosis
-
maple syrup urine disease
-
marble bone disease see osteopetrosis
-
Marchesani syndrome see Weill-Marchesani syndrome
-
Marchiafava-Micheli Syndrome see paroxysmal nocturnal hemoglobinuria
-
Marfan syndrome
-
Marie-Sainton syndrome see cleidocranial dysplasia
-
Marie-Struempell Disease see ankylosing spondylitis
-
Marinesco-Garland syndrome see Marinesco-Sjögren syndrome
-
Marinesco-Sjögren syndrome
-
marker X syndrome see fragile X syndrome
-
Marles-Greenberg-Persaud syndrome see Manitoba oculotrichoanal syndrome
-
Marles syndrome see Manitoba oculotrichoanal syndrome
-
Maroteaux-Lamy Syndrome see mucopolysaccharidosis type VI
-
Martin-Bell syndrome see fragile X syndrome
-
MAS see McCune-Albright syndrome
-
MASA syndrome see L1 syndrome
- MAT deficiency see beta-ketothiolase deficiency; hypermethioninemia
-
maternally inherited diabetes and deafness
-
matrin 3 distal myopathy see distal myopathy 2
-
Mayer-Rokitansky-Küster-Hauser-like syndrome see WNT4 Müllerian aplasia and ovarian dysfunction
-
Mayer-Rokitansky-Küster-Hauser syndrome
-
2-MBADD see 2-methylbutyryl-CoA dehydrogenase deficiency
-
2-MBCD deficiency see 2-methylbutyryl-CoA dehydrogenase deficiency
-
2-MBG see 2-methylbutyryl-CoA dehydrogenase deficiency
-
MBL deficiency see mannose-binding lectin deficiency
-
MBL2 deficiency see mannose-binding lectin deficiency
-
MBP deficiency see mannose-binding lectin deficiency
-
MCAD deficiency see medium-chain acyl-CoA dehydrogenase deficiency
-
MCADD see medium-chain acyl-CoA dehydrogenase deficiency
-
MCADH deficiency see medium-chain acyl-CoA dehydrogenase deficiency
-
McAlister dysplasia see atelosteogenesis type 2
-
McArdle disease see glycogen storage disease type V
-
McArdle syndrome see glycogen storage disease type V
-
McArdle type glycogen storage disease see glycogen storage disease type V
-
3-MCC see 3-methylcrotonyl-CoA carboxylase deficiency
-
MCC deficiency see 3-methylcrotonyl-CoA carboxylase deficiency
-
McCune-Albright syndrome
-
MCD deficiency see malonyl-CoA decarboxylase deficiency
-
MCHS see childhood myocerebrohepatopathy spectrum
-
MCKD2 see uromodulin-associated kidney disease
-
McKusick-Kaufman syndrome
-
McKusick's metaphyseal chondrodysplasia syndrome see cartilage-hair hypoplasia
-
MCL see hereditary leiomyomatosis and renal cell cancer
-
McLeod neuroacanthocytosis syndrome
-
MCOPS1 see Lenz microphthalmia syndrome
-
MCOPS2 see oculofaciocardiodental syndrome
-
MCOPS7 see microphthalmia with linear skin defects syndrome
-
MCPH see autosomal recessive primary microcephaly
-
MCPHA see Amish lethal microcephaly
-
MCT8 (SLC16A2)-specific thyroid hormone cell transporter deficiency see Allan-Herndon-Dudley syndrome
-
MCUL see hereditary leiomyomatosis and renal cell cancer
-
MDR3 deficiency see progressive familial intrahepatic cholestasis
-
MDS see Miller-Dieker syndrome
-
MEA see multiple endocrine neoplasia
-
MECD see Meesmann corneal dystrophy
-
Meckel syndrome
-
MECP2 duplication syndrome
-
MECP2-related severe neonatal encephalopathy
-
MED see multiple epiphyseal dysplasia
-
mediterranean anemia see beta thalassemia
-
Mediterranean Fever, Familial see familial Mediterranean fever
-
Mediterranean myoclonic epilepsy see Unverricht-Lundborg disease
-
medium-chain acyl-CoA dehydrogenase deficiency
-
Medullary cystic kidney disease type 2 see uromodulin-associated kidney disease
-
Meesmann corneal dystrophy
-
MEF see familial Mediterranean fever
-
Mega-epiphyseal dwarfism see otospondylomegaepiphyseal dysplasia
-
megalencephalic leukoencephalopathy with subcortical cysts
-
Meige lymphedema
-
MELAS see mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
-
MELAS Syndrome see mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
-
Melnick-Fraser syndrome see branchiootorenal syndrome
-
Melnick-Needles syndrome
-
membranoproliferative glomerulonephritis type II see dense deposit disease
-
MEMSA see myoclonic epilepsy myopathy sensory ataxia
-
MEN see multiple endocrine neoplasia
-
Ménière disease
-
Meniere's Disease see Ménière disease
-
Menkea syndrome see Menkes syndrome
-
Menkes syndrome
-
Mental Disorders
-
mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of the corpus callosum see FG syndrome
-
mental retardation-overgrowth syndrome see Simpson-Golabi-Behmel syndrome
-
Mental retardation with osteocartilaginous abnormalities see Coffin-Lowry syndrome
-
Mental Retardation, X-Linked
-
mental retardation, X-linked, with hypotonia see Allan-Herndon-Dudley syndrome
-
MEPOP see mitochondrial neurogastrointestinal encephalopathy disease
-
Meretoja syndrome see lattice corneal dystrophy type II
-
MERRF see myoclonic epilepsy with ragged-red fibers
-
MERRF Syndrome see myoclonic epilepsy with ragged-red fibers
-
mesomelic dwarfism of the hypoplastic ulna, fibula, and mandible type see Langer mesomelic dysplasia
-
mesomelic dwarfism-small genitalia syndrome see Robinow syndrome
-
MET see hypermethioninemia
-
Metabolic Disorders
-
metachromatic leukodystrophy
-
Metaphyseal chondrodysplasia, McKusick type see cartilage-hair hypoplasia
-
metaphyseal chondrodysplasia, recessive type see cartilage-hair hypoplasia
-
Metaphyseal chondrodysplasia, Shwachman type see Shwachman-Diamond syndrome
-
Metatropic dwarfism, type II see Kniest dysplasia
-
metatropic dysplasia
-
Metatropic dysplasia type II see Kniest dysplasia
-
Methemoglobinemia see methemoglobinemia, beta-globin type
-
methemoglobinemia, beta-globin type
-
2-methyl-3-hydroxybutyric aciduria see 17β-hydroxysteroid dehydrogenase type 10 deficiency
-
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency see 17β-hydroxysteroid dehydrogenase type 10 deficiency
-
2-methylbutyryl-CoA dehydrogenase deficiency
-
2-methylbutyryl-coenzyme A dehydrogenase deficiency see 2-methylbutyryl-CoA dehydrogenase deficiency
-
2-methylbutyryl glycinuria see 2-methylbutyryl-CoA dehydrogenase deficiency
-
3-methylcrotonyl-CoA carboxylase deficiency
-
3-methylcrotonyl-coenzyme A carboxylase deficiency see 3-methylcrotonyl-CoA carboxylase deficiency
-
Methylcrotonyl-CoA carboxylase deficiency see 3-methylcrotonyl-CoA carboxylase deficiency
-
3-methylcrotonylglycinuria see 3-methylcrotonyl-CoA carboxylase deficiency
-
3-methylglutaconic aciduria
-
3-Methylhydroxybutyric acidemia see beta-ketothiolase deficiency
-
methylmalonic acidemia
-
Meulengracht syndrome see Gilbert syndrome
-
mevalonate kinase deficiency
-
mevalonic aciduria see mevalonate kinase deficiency
-
mevalonicaciduria see mevalonate kinase deficiency
-
MFS see Marfan syndrome
-
MFT see multiple familial trichoepithelioma
-
MG see myasthenia gravis
-
MHAM see Cowden syndrome
-
MHBD deficiency see 17β-hydroxysteroid dehydrogenase type 10 deficiency
-
MHS - Malignant hyperthermia see malignant hyperthermia
-
Microangiopathic hemolytic anemia see thrombotic thrombocytopenic purpura
-
microcephalic osteodysplastic primordial dwarfism type II
-
Microcephaly
-
microcephaly, Amish type see Amish lethal microcephaly
-
Microcephaly, Mental Retardation, and Distinct Facial Features, with or without Hirschsprung disease see Mowat-Wilson syndrome
-
microcephaly-mesobrachyphalangy-tracheoesophageal fistula (MMT) syndrome see Feingold syndrome
-
microcephaly-oculo-digito-esophageal-duodenal (MODED) syndrome see Feingold syndrome
-
microcephaly primary hereditary see autosomal recessive primary microcephaly
-
microcytemia, beta type see beta thalassemia
-
1q21.1 microdeletion
-
9q22.3 microdeletion
-
9q34.3 microdeletion syndrome see Kleefstra syndrome
-
15q13.3 microdeletion
-
15q24 microdeletion
-
17q21.31 microdeletion syndrome
-
microphthalmia
-
Microphthalmia, cataracts, radiculomegaly, and septal heart defects see oculofaciocardiodental syndrome
-
microphthalmia or anophthalmos with associated anomalies see Lenz microphthalmia syndrome
-
microphthalmia, syndromic 1 see Lenz microphthalmia syndrome
-
Microphthalmia, syndromic 2 see oculofaciocardiodental syndrome
-
microphthalmia with linear skin defects syndrome
- microphthalmos see microphthalmia; microphthalmia with linear skin defects syndrome
-
Microsomal Triglyceride Transfer Protein Deficiency Disease see abetalipoproteinemia
-
MIDAS syndrome see microphthalmia with linear skin defects syndrome
-
MIDD see maternally inherited diabetes and deafness
-
Migraine
-
Migraine with Aura see familial hemiplegic migraine
-
milk sugar intolerance see lactose intolerance
-
Miller-Dieker syndrome
-
Miller syndrome
-
Milroy disease
-
Minicore disease see multiminicore disease
-
Minicore myopathy see multiminicore disease
-
MIRAS see ataxia neuropathy spectrum
-
misalignment of the pulmonary vessels see alveolar capillary dysplasia with misalignment of pulmonary veins
-
Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated see beta-ketothiolase deficiency
-
Mitochondrial acetoacetyl-CoA thiolase deficiency see beta-ketothiolase deficiency
-
mitochondrial aspartyl-tRNA synthetase deficiency see leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
-
mitochondrial complex IV deficiency see cytochrome c oxidase deficiency
-
Mitochondrial Diseases
-
mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria see succinate-CoA ligase deficiency
-
mitochondrial DNA depletion syndrome 6 see MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
-
mitochondrial DNA depletion syndrome, encephalomyopathic form, with mild methylmalonic aciduria see succinate-CoA ligase deficiency
-
mitochondrial DNA depletion syndrome, hepatocerebral form see deoxyguanosine kinase deficiency
-
mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
-
mitochondrial inherited diabetes and deafness see maternally inherited diabetes and deafness
-
Mitochondrial Myopathies
-
mitochondrial neurogastrointestinal encephalopathy disease
-
mitochondrial recessive ataxia syndrome see ataxia neuropathy spectrum
-
mitochondrial trifunctional protein deficiency
-
MJD see spinocerebellar ataxia type 3
-
MK see Menkes syndrome
- MKS see McKusick-Kaufman syndrome; Meckel syndrome
-
ML III see mucolipidosis III alpha/beta
-
ML IIIC see mucolipidosis III gamma
-
ML4 see mucolipidosis type IV
-
MLC see megalencephalic leukoencephalopathy with subcortical cysts
-
MLD see metachromatic leukodystrophy
-
MLII see mucolipidosis II alpha/beta
-
MLIV see mucolipidosis type IV
-
MLS syndrome see microphthalmia with linear skin defects syndrome
-
MMA see methylmalonic acidemia
-
MmD see multiminicore disease
-
MNGIE disease see mitochondrial neurogastrointestinal encephalopathy disease
-
MNGIE syndrome see mitochondrial neurogastrointestinal encephalopathy disease
-
MNK see Menkes syndrome
-
MNS see Melnick-Needles syndrome
-
Möbius sequence see Moebius syndrome
-
Mobius syndrome see Moebius syndrome
-
Moebius syndrome
-
Mohr-Tranebjærg syndrome see deafness-dystonia-optic neuronopathy syndrome
-
molluscum fibrosum see juvenile hyaline fibromatosis
-
monilethrix
-
monocarboxylate transporter 8 (MCT8) deficiency see Allan-Herndon-Dudley syndrome
-
monosaccharide malabsorption see glucose-galactose malabsorption
-
monosomy 1p36 syndrome see 1p36 deletion syndrome
-
monosomy 4p see Wolf-Hirschhorn syndrome
-
monosomy 5p see cri-du-chat syndrome
-
17p11.2 monosomy see Smith-Magenis syndrome
-
monosomy 17q21.31 see 17q21.31 microdeletion syndrome
-
monosomy 22q13 see 22q13.3 deletion syndrome
-
monosomy X see Turner syndrome
-
MOPD2 see microcephalic osteodysplastic primordial dwarfism type II
-
MOPDII see microcephalic osteodysplastic primordial dwarfism type II
-
morbus Dercum see adiposis dolorosa
-
Morquio-Brailsford disease see mucopolysaccharidosis type IV
-
Morquio Disease see mucopolysaccharidosis type IV
-
Morquio Syndrome see mucopolysaccharidosis type IV
-
Morvan disease see hereditary sensory and autonomic neuropathy type II
-
Moschkowitz Disease see thrombotic thrombocytopenic purpura
-
MOTA see Manitoba oculotrichoanal syndrome
-
moth-eaten skeletal dysplasia see Greenberg dysplasia
-
motor neuron disease, amyotrophic lateral sclerosis see amyotrophic lateral sclerosis
-
Mount-Reback syndrome see familial paroxysmal nonkinesigenic dyskinesia
-
Movement Disorders
-
Mowat-Wilson syndrome
-
Moynahan syndrome see multiple lentigines syndrome
-
MPD1 see Laing distal myopathy
-
MPD2 see distal myopathy 2
-
MPGNII see dense deposit disease
-
MPRM see hereditary myopathy with early respiratory failure
-
MPS I see mucopolysaccharidosis type I
-
MPS II see mucopolysaccharidosis type II
-
MPS III see mucopolysaccharidosis type III
-
MPS IV see mucopolysaccharidosis type IV
-
MPS VI see mucopolysaccharidosis type VI
-
MPS VII see mucopolysaccharidosis type VII
-
MPS6 see mucopolysaccharidosis type VI
-
MPS7 see mucopolysaccharidosis type VII
-
MPV17-associated hepatocerebral MDS see MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
-
MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
-
MRI Scans see Leigh syndrome
-
MRKH syndrome see Mayer-Rokitansky-Küster-Hauser syndrome
-
MSA see multiple system atrophy
-
3-MSBN see 3-M syndrome
-
MSS see Marinesco-Sjögren syndrome
-
MSUD see maple syrup urine disease
-
MTDPS6 see MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
-
MTMX see X-linked myotubular myopathy
-
MTP deficiency see mitochondrial trifunctional protein deficiency
-
Muckle-Wells syndrome
-
mucocutaneous lymph node syndrome see Kawasaki disease
-
mucocutaneous venous malformations see multiple cutaneous and mucosal venous malformations
-
mucolipidosis I see sialidosis
-
mucolipidosis II alpha/beta
-
mucolipidosis III alpha/beta
-
mucolipidosis III gamma
-
mucolipidosis type I see sialidosis
-
mucolipidosis type IV
-
mucopolysaccharidosis type I
-
mucopolysaccharidosis type II
-
mucopolysaccharidosis type III
-
mucopolysaccharidosis type IV
-
mucopolysaccharidosis type VI
-
mucopolysaccharidosis type VII
-
mucoviscidosis see cystic fibrosis
-
Muenke syndrome
-
Mullerian aplasia see Mayer-Rokitansky-Küster-Hauser syndrome
-
Mullerian aplasia and hyperandrogenism see WNT4 Müllerian aplasia and ovarian dysfunction
-
Müllerian duct failure see WNT4 Müllerian aplasia and ovarian dysfunction
-
Mullerian dysgenesis see Mayer-Rokitansky-Küster-Hauser syndrome
-
Multi-Infarct Dementia see cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Multi-minicore disease see multiminicore disease
-
Multicore disease see multiminicore disease
-
Multicore myopathy see multiminicore disease
-
multiminicore disease
-
Multiple acyl-CoA dehydrogenase deficiency see glutaric acidemia type II
-
multiple angiomas and endochondromas see Maffucci syndrome
-
Multiple Carboxylase Deficiency
-
Multiple Carboxylase Deficiency, Late-Onset see biotinidase deficiency
-
Multiple Carboxylase Deficiency, Neonatal Form see holocarboxylase synthetase deficiency
-
multiple cartilaginous exostoses see hereditary multiple exostoses
-
multiple cutaneous and mucosal venous malformations
-
multiple cutaneous and uterine leiomyomata see hereditary leiomyomatosis and renal cell cancer
-
multiple cutaneous leiomyoma see hereditary leiomyomatosis and renal cell cancer
-
multiple endocrine neoplasia
-
multiple epiphyseal dysplasia
-
multiple FAD dehydrogenase deficiency see glutaric acidemia type II
-
multiple familial trichoepithelioma
-
multiple hamartoma syndrome see Cowden syndrome
-
multiple hereditary exostoses see hereditary multiple exostoses
-
multiple lentigines syndrome
-
multiple osteochondromas see hereditary multiple exostoses
-
multiple osteochondromatosis see hereditary multiple exostoses
-
multiple pterygium syndrome
-
multiple sebaceous cysts see steatocystoma multiplex
-
multiple system atrophy
-
multiplex steatocystoma see steatocystoma multiplex
-
Murray syndrome see juvenile hyaline fibromatosis
-
Muscle Cramps see hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
-
Muscle Disorders
-
muscle glycogen phosphorylase deficiency see glycogen storage disease type V
-
Muscle hypertrophy syndrome see myostatin-related muscle hypertrophy
-
muscle phosphorylase deficiency see glycogen storage disease type V
-
Muscular Dystrophy
-
Muscular dystrophy, congenital, Fukuyama type see Fukuyama congenital muscular dystrophy
-
Muscular dystrophy, congenital progressive, with mental retardation see Fukuyama congenital muscular dystrophy
-
Muscular dystrophy, congenital, with central nervous system involvement see Fukuyama congenital muscular dystrophy
-
muscular dystrophy, Duchenne and Becker types see Duchenne and Becker muscular dystrophy
-
Muscular Dystrophy, Emery-Dreifuss see Emery-Dreifuss muscular dystrophy
-
Muscular Dystrophy, Facioscapulohumeral see facioscapulohumeral muscular dystrophy
-
Muscular Dystrophy, Landouzy Dejerine see facioscapulohumeral muscular dystrophy
-
Muscular dystrophy, limb-girdle, with Paget disease of bone see inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
-
Muscular Dystrophy, Oculopharyngeal see oculopharyngeal muscular dystrophy
-
muscular dystrophy, pseudohypertrophic see Duchenne and Becker muscular dystrophy
-
mutilating keratoderma see Vohwinkel syndrome
- MWS see Mowat-Wilson syndrome; Muckle-Wells syndrome
-
myasthenia gravis
-
myelinosis centralis diffusa see leukoencephalopathy with vanishing white matter
-
Myelodysplastic Syndromes
-
myelofibrosis with myeloid metaplasia see primary myelofibrosis
-
myeloid leukemia, acute, M3 see acute promyelocytic leukemia
-
myeloid metaplasia see primary myelofibrosis
-
MYH-associated polyposis see familial adenomatous polyposis
-
MYH9-related disorder
-
MYH9RD see MYH9-related disorder
-
Myhre-Riley-Smith syndrome see Bannayan-Riley-Ruvalcaba syndrome
-
Myhre syndrome
-
myoadenylate deaminase deficiency see adenosine monophosphate deaminase deficiency
-
myoclonic dystonia see myoclonus-dystonia
-
Myoclonic Epilepsies, Progressive
-
myoclonic epilepsy myopathy sensory ataxia
-
myoclonic epilepsy of Lafora see Lafora progressive myoclonus epilepsy
-
myoclonic epilepsy of Unverricht and Lundborg see Unverricht-Lundborg disease
-
Myoclonic epilepsy with choreoathetosis see dentatorubral-pallidoluysian atrophy
-
myoclonic epilepsy with ragged-red fibers
-
myoclonus cherry red spot syndrome see sialidosis
-
myoclonus-dystonia
-
Myoencephalopathy ragged-red fiber disease see myoclonic epilepsy with ragged-red fibers
-
myofibrillar myopathy
-
myoglobinuria due to abnormal glycolysis see myopathy with deficiency of iron-sulfur cluster assembly enzyme
-
Myoneurogastrointestinal encephalopathy syndrome see mitochondrial neurogastrointestinal encephalopathy disease
-
myopathia distalis type 2 see distal myopathy 2
-
myopathic limb-girdle syndrome see limb-girdle muscular dystrophy
-
myopathies, nemaline see nemaline myopathy
-
Myopathies, Structural, Congenital
-
Myopathy, Central Core see central core disease
-
myopathy due to phosphoglycerate mutase deficiency see phosphoglycerate mutase deficiency
-
Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke see mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
-
myopathy, nemaline see nemaline myopathy
-
myopathy, proximal, with early respiratory muscle involvement see hereditary myopathy with early respiratory failure
-
myopathy with deficiency of iron-sulfur cluster assembly enzyme
-
myophosphorylase deficiency see glycogen storage disease type V
-
Myositis
-
Myositis Ossificans see fibrodysplasia ossificans progressiva
-
myostatin-related muscle hypertrophy
-
myotonia atrophica see myotonic dystrophy
-
myotonia congenita
-
myotonia dystrophica see myotonic dystrophy
-
Myotonic Disorders
-
myotonic dystrophy
-
myotubular myopathy see centronuclear myopathy
-
Myxedema, Congenital see congenital hypothyroidism
| |