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ГЕНЕТИЧЕСКИЕ ИССЛЕДОВАНИЯ
 
 

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
M
  • MAD Deficiency
  • MADA Deficiency
  • MASA syndrome
  • MCM deficiency
  • MELAS syndrome
  • MERRF syndrome
  • MES
  • MET Protooncogene (MET)
  • MIC5
  • MMA due to MCM deficiency
  • MODY, Glucokinase-related
  • MODY, Type I
  • MODY, Type II
  • MPI deficiency
  • MTC1
  • MTCF
  • MTHFR deficiency, thermolabile type
  • Machado-Joseph Disease (MJD)
  • Macrocephaly, multiple lipomas and heman
  • Macrocephaly, pseudopapilledema, and mul
  • Macrothrombocytopenia, familial, Bernard
  • Macular degeneration, juvenile
  • Macular degeneration, polymorphic vitell
  • Macular dystrophy with flecks, type 1
  • Macular dystrophy, butterfly-shaped pigm
  • Macular dystrophy, vitelliform (VMD2)
  • Madelung deformity
  • Major Alpha-globin locus
  • Major Histocompatibility Complex, Class
  • Major Histocompatibility Complex, Class
  • Major Histocompatibility Complex, Class
  • Major alpha-globin locus
  • Major histocompatibility complex class I
  • Major histocompatibility complex, class
  • Male Turner syndrome
  • Male pseudohermaphroditism due to 5-alph
  • Malignant hyperthermia
  • Malignant hyperthermia susceptibility 1
  • Malignant tumors of the central nervous
  • Mannosephosphate isomerase deficiency
  • Marble bones, autosomal dominant
  • Marble bones, autosomal recessive (OPTB1)
  • Marenostrin
  • Marfan Syndrome (MFS)
  • Marfan Syndrome, type I (MFS1)
  • Marfan syndrome type II (MFS2)
  • Marfan-like connective tissue disorder
  • Marie-Strumpell Spondylitis
  • Marker X syndrome
  • Martin-Bell syndrome
  • Mason-type diabetes
  • Maturity onset diabetes of the young, ty
  • Maturity-onset diabetes of the young MO
  • Maturity-onset diabetes of the young, Ty
  • Maturity-onset diabetes of the young, Ty
  • Maturity-onset diabetes of the young, Ty
  • Maturity-onset diabetes of the young, Ty
  • McArdle syndrome, autosomal dominant
  • McCune-Albright syndrome
  • Mcardle disease
  • Meckel syndrome (MKS)
  • Meckel syndrome, type 1 (MKS1)
  • Meckel-Gruber syndrome
  • Med, autosomal recessive
  • Medium-chain acyl-CoA dehydrogenase (MCA)
  • Medullary cystic kidney disease, autosom
  • Medullary thyroid carcinoma, familial
  • Medullary thyroid carcinoma, familial M
  • Megacolon, aganglionic (MGC)
  • Melanocortin 2 receptor (MC2R)
  • Melanodermic leukodystrophy
  • Melanoma cutaneous malignant, 3 (CMM3)
  • Melanoma, Cutaneous Malignant (CMM1)
  • Melanoma, Cutaneous Malignant, 2 (CMM2)
  • Melanoma, familial (MLM)
  • Melanoma, malignant
  • Melnick-Fraser syndrome
  • Menin
  • Menkes syndrome (MK; MNK)
  • Mental retardation syndrome
  • Mental retardation, X-linked non specifi
  • Mental retardation, X-linked nonspecific
  • Mental retardation, X-linked, 21 (MRX21)
  • Mental retardation, X-linked, associated
  • Mental retardation, X-linked, associated
  • Mental retardation, aphasia, shuffling g
  • Mental retardation, unusual facies
  • Menzel type OPCA
  • Mephenytoin 4-prime-hydroxylase
  • Mephenytoin hydroxylation, defect
  • Mercaptopurine-6 sensitivity
  • Meretoja type amyloidosis
  • Merlin
  • Mesangial scleroris, diffuse (DMS)
  • Mesangial sclerosis, familial
  • Mesangial sclerosis, isolated diffuse I
  • Mesiodens-cataract syndrome
  • Metachromatic leukodystrophy (MLD)
  • Metachromatic leukodystrophy due to defi
  • Metachromatic leukoencephalopathy
  • Metaphyseal chondrodysplasia, McKusick t
  • Metaphyseal chondrodysplasia, Schmid typ
  • Metatropic dwarfism, type II
  • Metatropic dysplasia II
  • Methemoglobinemia, Alpha-globin type
  • Methemoglobinemia, beta-globin type
  • Methyl-CpG-Binding Protein 2 (MECP2)
  • Methylcrotonyl-3-CoA carboxylase 1 defic
  • Methylcrotonylglycinuria-3 I
  • Methylenetetrahydrofolate reductase defi
  • Methylenetetrahydrofolate-5,10 reductase
  • Methylmalonicaciduria due to methylmalon
  • Methylmalonicadiduria due to MCM deficie
  • Methylmalonyl CoA mutase (MUT)
  • Microcephaly with normal intelligence, i
  • Microphatalmia, dermal aplasia, and scle
  • Microphtalmia with linear skin defects
  • Micropolygyria with muscular dystrophy
  • Microsomal triglyceride transfer protein
  • Midas syndrome
  • Mild juvenile diabetes mellitus
  • Miller-Dieker lissencephaly syndrome MD
  • Miller-Dieker syndrome chromosome region
  • Mimimum potassium ion channel-related pe
  • Minimal potassium channel, MINK
  • Mink-related peptide 1
  • Minor Alpha-globin locus
  • Minor histocompatibility antigen HA-2
  • Minus-4.1 trait
  • Mitochondiral DNA depletion syndrome, he
  • Mitochondrial DNA breakage syndrome
  • Mitochondrial DNA depletion myopathy
  • Mitochondrial DNA depletion syndrome
  • Mitochondrial Encephalomyopathies
  • Mitochondrial Myopathies
  • Mitochondrial NADH dehydrogenase compone
  • Mitochondrial complex I deficiency
  • Mitochondrial cytopathy
  • Mitochondrial disorders
  • Mitochondrial fatty acid oxidation, comb
  • Mitochondrial myopathy
  • Mitochondrial myopathy, encephalopathy,
  • Mitochondrial trifunctional protein, alp
  • Mohr-Tranebjaerg syndrome (MTS)
  • Morquio syndrome B
  • Mucopolysaccharidosis type I (MPS 1)
  • Mucopolysaccharidosis type IIIA (MPS3A)
  • Mucopolysaccharidosis type IIIB (MPS3B)
  • Mucopolysaccharidosis type IVB (MPS4B)
  • Mucopolysaccharidosis type VII (MPS VII);
  • Mucopolysaccharisosis type II (MPS2)
  • Mucosal neuroma syndrome
  • Mucoviscidosis
  • Muenke nonsyndromic coronal craniosynost
  • Muenke syndrome
  • Muir-Torre Syndrome (MTS)
  • Mulibrey Nanism Gene (MUL)
  • Multiple Endocrine Neoplasia type 1 (MEN
  • Multiple Endocrine Neoplasia type II (ME
  • Multiple Endocrine Neoplasia type II B
  • Multiple Hamartoma syndrome (MHAM)
  • Multiple basal cell nevi, odontogenic ke
  • Multiple cartilaginous exostoses
  • Multiple endocrine neoplasia, type IIA
  • Multiple endocrine neoplasia, type IIB
  • Multiple endocrine neoplasia, type III
  • Multiple epiphyseal dysplasia, autosomal
  • Multiple exostoses with spastic tetrapar
  • Multiple osteochondromatosis
  • Multiple tumor suppressor 1 (MTS1)
  • Muscle glycogen phosphorylase deficiency
  • Muscular Dystrophy, Duchenne-like (DMDA)
  • Muscular Dystrophy, Limb-Girdle, type 2D
  • Muscular atrophy, adult spinal (SMA4)
  • Muscular atrophy, juvenile
  • Muscular atrophy, spinal, infantile chro
  • Muscular atrophy, spinal, intermediate t
  • Muscular dystrophy, Limb-Girdle, type 2
  • Muscular dystrophy, Limb-Girdle, type 2A
  • Muscular dystrophy, Limb-Girdle, type 2B
  • Muscular dystrophy, Limb-Girdle, type 2C
  • Muscular dystrophy, Limb-Girdle, type 2F
  • Muscular dystrophy, Limb-Girdle, type 3
  • Muscular dystrophy, congenital progressi
  • Muscular dystrophy, congenital, Fukuyama
  • Muscular dystrophy, congenital, with cen
  • Muscular dystrophy, facioscapulohumeral
  • Muscular dystrophy, facioscapulohumeral,
  • Muscular dystrophy, oculopharyngeal
  • Muscular dystrophy, oculopharyngeal auto
  • Muscular dystrophy, pelvofemoral
  • Muscular dystrophy, pseudohypertrophic p
  • Muscular dystrophy; tardive, Dreifuss-Em
  • Muscular-atrophy, infantile
  • MutL, E. coli, homolog of, 1 (MLH1)
  • MutS, E. Coli, Homolog of, 6 (MSH6)
  • MutS, E. Coli, homolog of, 6 (MSH6)
  • MutS, E. coli, homolog of, 2 (MSH2)
  • Mutated in multiple advanced cancers 1
  • Myasthenia Gravis, Familial Infantile F
  • Myasthenia gravis, autosomal recessive
  • Myasthenia gravis, familial infantile, 2
  • Myasthenia, congenital
  • Myelin glycoprotein p-zero P(0)
  • Myelin protein zero (MPZ)
  • Myelin protein, peripheral (MPP)
  • Myoadenylate Deaminase Deficiency, myopa
  • Myoclonic epilepsy associated with ragge
  • Myoclonic epilepsy of Lafora (MELF)
  • Myoclonic epilepsy of Unverricht and Lun
  • Myoclonic epilepsy with choreoathetosis
  • Myokymia with periodic ataxia
  • Myolecytic leukemia-like syndrome, famil
  • Myoneurogastrointestinal encephalopathy
  • Myopathy with deficiency of carnitine
  • Myopathy, centronuclear (CNM)
  • Myopathy, mitochondrial, with deficiency
  • Myophosphorylase deficiency
  • Myosin VIIA (MYO7A)
  • Myosin, cardiac, heavy chain, beta (MYHC
  • Myosin, heavy chain 7, cardiac muscle, b
  • Myosin, uniconventionnal, Family VII,
  • Myosin-binding protein C, cardiac (MYBPC)
  • Myotonia congenita, atypical, acetazolam
  • Myotonia congenita, autosomal dominant
  • Myotonia congenita, autosomal recessive
  • Myotonia congenita, autosomal recessive,
  • Myotonia, generalized
  • Myotonic dystrophy 1
  • Myotonic dystrophy 2
  • Myotonic myopathy, proximal
  • Myotubular myopathy 1 (MTM1)
  • Myotubular myopathy, X-linked (MTMX; XLM)
  • Myotubularin
  • Myxoma, spotty pigmentation, and encocri
  • Myxoma-adrenocortical dysplasia syndrome
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z