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Hormonal, Nutritional, Metabolic, and Immune Disorders M
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Hormonal, Nutritional, Metabolic, and Immune Disorders M
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Hormonal, Nutritional, Metabolic, and Immune Disorders
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Hormonal, Nutritional, Metabolic, and Immune Disorders M
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Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders M
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Name
Category
2-methyl-3-hydroxybutyric acidemia
3-MCC deficiency
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
macronodular adrenal cortical hyperplasia
MADD
Madelung's disease
magnesium deficiency
magnesium deficiency tetany syndrome
magnesium excess
magnesium loss, isolated renal
magnesium metabolism disorder
magnesium overload
magnesium transport defect, renal tubular
magnesium wasting, renal
malabsorption syndrome, lysine
malabsorption syndrome, methionine
malabsorption, congenital sucrose-isomaltose
malabsorption, familial methionine
malabsorption, glucose-galactose
malabsorption, intestinal disaccharidase deficiency or
malabsorption, lactose
malabsorption, monosaccharide
malabsorption, tryptophan
malabsorptive diarrhea, congenital
male central precocious puberty
male climacteric
male delayed puberty
male hypogonadism, primary
male menopause
male precocious puberty
male puberty, precocious
malignant arginosucinic aciduria
malignant malnutrition
malnutrition
malnutrition, caloric
malnutrition, energy
malnutrition, hypoalbuminemic protein-energy
malnutrition, malignant
malnutrition, protein
malnutrition, protein-energy
malnutrition, unspecified, protein-calorie
malnutrition, unspecified, severe
maltase deficiency, acid
mannosidosis
mannosidosis, lysosomal alpha B
mannosidosis, lysosomal beta A
maple syrup urine disease
maple syrup urine disease, Type III
marasmic kwashiorkor
marasmus
marble brain disease
Maroteaux-Lamy disease
Maroteaux-Lamy syndrome
MAT deficiency
MCADD
McArdle disease
McArdle's disease
MCC deficiency
MCD
MCD, early-onset
MCD, early-onset carboxylase deficiency neonatal
MCD, juvenile-onset
MCD, late-onset
Mediterranean fever, familial
medium chain acyl-CoA dehydrogenase deficiency
medullary hyperfunction, adrenal
medullary hyperplasia, adrenal
medullary hypofunction, adrenal
medullary insufficiency, adrenal
medullary nephrocalcinosis
medulloadrenal hyperfunction
medulloadrenal hypofunction
medulloadrenal insufficiency
megaloblastic anemia, cblE-type homocystinuria and
megaloblastic anemia, cblG-type homocystinuria and
melanoderma, Addison's
melanodermic leukodystrophy
melasma addisonii
mellitus with optic atrophy and deafness, diabetes insipidus and
menarche, delayed
Menke's kinky hair disease
Menkes syndrome
menopause, male
metabolic acidosis
metabolic acidosis, high-anion-gap
metabolic acidosis, hyperchloremic
metabolic acidosis, hyperkalemic normal-anion-gap
metabolic acidosis, hypokalemic normal-anion-gap
metabolic acidosis, normal-anion-gap
metabolic alkalosis
metabolic alkalosis, chloride-resistant
metabolic alkalosis, chloride-responsive
metabolic alkalosis, hypochloremic
metabolic syndrome
metabolic syndrome X
metabolism disorder, calcium
metabolism disorder, cobalamin
metabolism disorder, copper
metabolism disorder, cystathionine
metabolism disorder, glucose
metabolism disorder, glutaric acid
metabolism disorder, histidine
metabolism disorder, iron
metabolism disorder, lipoid
metabolism disorder, magnesium
metabolism disorder, methionine
metabolism disorder, porphyrin
metabolism disorder, proline
metabolism disorder, sulfur-bearing amino-acid
metabolism disorder, unspecified, amino-acid
metabolism disorder, unspecified, lysine
metabolism disorder, unspecified, phosphorus
metabolism disorder, unspecified, plasma protein
metabolism disorder, urea cycle
metabolism disturbance, branched-chain amino acid
metabolism disturbance, isoleucine
metabolism disturbance, leucine
metabolism disturbance, valine
metabolism, disorder of carbohydrate transport and
metabolism, intermittent ataxia with abnormal pyruvate
methionine adenosyltransferase deficiency
methionine malabsorption syndrome
methionine malabsorption, familial
methionine metabolism disorder
methylcobalamin deficiency, cblE-type
methylmalonic acidemia
methylmalonic acidemia and homocystinuria, cblC-type
methylmalonic acidemia and homocystinuria, cblD-type
methylmalonic acidemia and homocystinuria, cblF-type
methylmalonic acidemia, cblA-type
methylmalonic acidemia, cblB-type
methylmalonic aciduria
methylmalonic aciduria and homocystinura, cblD-type
methylmalonic aciduria and homocystinuria, cblC-type
methylmalonic aciduria and homocystinuria, cblC-type vitamin B12-responsive
methylmalonic aciduria and homocystinuria, cblF-type
methylmalonic aciduria, cblA-type
methylmalonic aciduria, cblA-type vitamin B12-responsive
methylmalonic aciduria, cblB-type
methylmalonic aciduria, cblB-type vitamin B12-responsive
methylmalonic aciduria, mut-type
methylmalonyl-CoA mutase and homocysteine:methyltetrahydrofolate methyltransferase, combined deficiency of
methylmalonyl-CoA mutase deficiency
methyloxidase deficiency, familial
methyloxidase deficiency, Type I corticosterone
methyloxidase deficiency, Type II corticosterone
methyltransferase, combined deficiency of methylmalonyl-CoA mutase and homocysteine:methyltetrahydrofolate
Mg deficiency
Mg excess
Mg overload
MGCA
MGUS
micronodular adrenal coritcal hyperplasia
microsomal triglyceride transfer protein deficiency
microvillous atrophy, congenital
microvillous inclusion disease
mild hypophosphatasia
milk allergy
milk intolerance
mineralocorticoid-excess adrenal cortical hyperfunction
mitochondrial acetoacetyl-CoA thiolase deficiency
mixed hyperlipidemia
MK
ML I
ML II
ML III
MNK
MOCOD
molybdenum cofactor deficiency
moniliasis, hypoadrenocorticism with hypoparathyroidism and superficial
monoclonal gammopathy
monoclonal gammopathy of unknown significance
monoclonal gammopathy, asymptomatic
monoclonal gammopathy, benign
monoclonal gammopathy, idiopathic
monoclonal gammopathy, transient
monophosphate synthase deficiency, uridine
monophosphate synthetase deficiency, uridine
monosaccharide malabsorption
morbus Teutschlaender
Morquio disease
Morquio syndrome
Morquio syndrome A
Morquio syndrome B
Morquio syndrome, Type A
Morquio syndrome, Type B
Morsier, dysplasia olfactogenitalis of de
MPS I
MPS IHS
MPS II
MPS IIIA
MPS IIIB
MPS IIIC
MPS IIID
MPS IVB
MPS V
MPS VI
MPS VII
MPS1-H
MPS1-S
MPS2
MPS3A
MPS3B
MPS3C
MPS4A
MPS4B
MPS5
MPS6
MPS7
MPSIVA
MSL
MSUD
MTP deficiency
mu heavy chain disease
mucolipidosis
mucolipidosis III
mucolipidosis IIIA
mucolipidosis, Type I
mucolipidosis, Type II
mucolipidosis, Type III
mucolipidosis, Type IV
mucopolysaccharidosis
mucopolysaccharidosis, Type I
mucopolysaccharidosis, Type IH
mucopolysaccharidosis, Type IHS
mucopolysaccharidosis, Type II
mucopolysaccharidosis, Type III
mucopolysaccharidosis, Type IIIA
mucopolysaccharidosis, Type IIIB
mucopolysaccharidosis, Type IIIC
mucopolysaccharidosis, Type IIID
mucopolysaccharidosis, Type IS
mucopolysaccharidosis, Type IV
mucopolysaccharidosis, Type IVA
mucopolysaccharidosis, Type IVB
mucopolysaccharidosis, Type V
mucopolysaccharidosis, Type VI
mucopolysaccharidosis, Type VII
mucoviscidosis
multifocal eosinophilic granuloma
multifocal Langerhans cell histiocytosis
multifocal LCH
multinodular goiter, toxic
multiple acyl CoA dehydrogenase deficiency
multiple carboxylase deficiency
multiple carboxylase deficiency, juvenile-onset
multiple carboxylase deficiency, late-onset
multiple carboxylase deficiency, neonatal
multiple symmetric lipomatosis
muscle glycogen disease
muscle glycogen phosphorylase deficiency
muscle phosphofructokinase deficiency
muscle phosphoglycerate mutase deficiency
mut-type methylmalonic aciduria
mutase and homocysteine:methyltetrahydrofolate methyltransferase, combined deficiency of methylmalonyl-CoA
mutase deficiency, methylmalonyl-CoA
mutase deficiency, muscle phosphoglycerate
mutations, familial partial lipodystrophy associated with PPARG
MVID
myoclonus syndrome, cherry red spot-
myoclonus-cherry red spot syndrome
myopathic carnitine deficiency
myopathy, phosphofructokinase
myophosphorylase deficiency
myxedema
myxedema coma
myxedema crisis
myxedema, primary