Genetic Conditions - M

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Genetic Conditions…

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Male Breast Cancer see breast cancer

Male Genital Disorders

Male Turner Syndrome see Noonan syndrome

Malignant neoplasm of breast see breast cancer

malignant tumor of breast see breast cancer

Malignant tumor of urinary bladder see bladder cancer

Mammary cancer see breast cancer

maple syrup urine disease

Marfan syndrome

Marker X syndrome see fragile X syndrome

Martin-Bell Syndrome see fragile X syndrome

MCAD deficiency see medium-chain acyl-coenzyme A dehydrogenase deficiency

MCADD see medium-chain acyl-coenzyme A dehydrogenase deficiency

MCADH deficiency see medium-chain acyl-coenzyme A dehydrogenase deficiency

McAlister dysplasia see atelosteogenesis, type 2

MEA Type I see multiple endocrine neoplasia type 1

Mediterranean Anemia see beta thalassemia

Mediterranean Fever, Familial see familial Mediterranean fever

medium-chain acyl-coenzyme A dehydrogenase deficiency

Mega-epiphyseal dwarfism see otospondylomegaepiphyseal dysplasia

MEN 1 see multiple endocrine neoplasia type 1

MEN 2 see multiple endocrine neoplasia type 2

MEN I see multiple endocrine neoplasia type 1

MEN II see multiple endocrine neoplasia type 2

Menkea syndrome see Menkes syndrome

Menkes syndrome

Mental retardation with osteocartilaginous abnormalities see Coffin-Lowry syndrome

Metabolic Disorders

Metatropic dwarfism, type II see Kniest dysplasia

Metatropic dysplasia type II see Kniest dysplasia

methemoglobinemia, beta-globin type

methylmalonic acidemia

MFS see Marfan syndrome

MHAM see Cowden syndrome

mitochondrial trifunctional protein deficiency

MK - Menkes syndrome see Menkes syndrome

MMA see methylmalonic acidemia

MNK - Menkes syndrome see Menkes syndrome

monosomy X see Turner syndrome

Motor Neuron Disease, Amyotrophic Lateral Sclerosis see amyotrophic lateral sclerosis

Movement Disorders

MSUD see maple syrup urine disease

MTP deficiency see mitochondrial trifunctional protein deficiency

Mucoviscidosis see cystic fibrosis

Muenke syndrome

Multi-Infarct Dementia see CADASIL

Multiple Carboxylase Deficiency, Late-Onset see biotinidase deficiency

multiple endocrine neoplasia type 1

multiple endocrine neoplasia type 2

Multiple epiphyseal dysplasia, autosomal recessive see recessive multiple epiphyseal dysplasia

Multiple hamartoma syndrome see Cowden syndrome

Multiple neurofibromatosis see neurofibromatosis

Muscular Dystrophy

muscular dystrophy, Duchenne and Becker types

Myotonia atrophica see myotonic dystrophy

Myotonia dystrophica see myotonic dystrophy

myotonic dystrophy

Myxedema, Congenital see congenital hypothyroidism