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Hormonal, Nutritional, Metabolic, and Immune Disorders L
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Hormonal, Nutritional, Metabolic, and Immune Disorders L
DESCIPHER HEALTH ➤
Diseases
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Hormonal, Nutritional, Metabolic, and Immune Disorders
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Hormonal, Nutritional, Metabolic, and Immune Disorders L
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Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders L
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Name
Category
L-lysine:NAD-oxido-reductase deficiency
L-xylulose reductase deficiency
L-xylulosuria
lack of fluids
lack of thirst
lactase deficiency, adult
lactase deficiency, congenital
lactase nonpersistence
lactate dehydrogenase A deficiency
lactate dehydrogenase B deficiency
lactate dehydrogenase deficiency
lactic acidosis
lactic acidosis I, ataxia with
lactic acidosis II, ataxia with
lactose intolerance
lactose intolerance, adult-type
lactose intolerance, familial
lactose malabsorption
lactoside lipidosis, ceramide
lactosyl ceramidosis
Langerhans cell histiocytosis
Langerhans cell histiocytosis, multifocal
Lanois-Bensaude syndrome
Laron syndrome
Laron Type I dwarfism
late effect of rickets
late-onset 21-hydroxylase deficiency
late-onset 3-beta-hydroxysteroid dehydrogenase deficiency
late-onset ADA-SCID
late-onset adenosine-deaminase-deficiency severe combined immunodeficiency
late-onset argininosuccinic aciduria
late-onset carbamyl phosphate synthetase deficiency
late-onset hypogammaglobulinemia
late-onset juvenile nephropathic cystinosis
late-onset MCD
late-onset multiple carboxylase deficiency
late-onset N-acetylglutamate synthase deficiency
late-onset ornithine transcarbamylase deficiency
Launois-Cleret syndrome
LCAH
LCAT deficiency
LCATA deficiency
LCDD
LCH
LCH, multifocal
LDHA deficiency
LDHB deficiency
LDHBD
LDL deficiency
LDL hyperlipoproteinemia
LDL receptor disorder
lecithin-cholesterol acyltransferase deficiency
leprechaunism
Lesch-Nyhan syndrome
leucine metabolism disturbance
leucine-induced hypoglycemia
leucine-sensitive hypoglycemia, idiopathic
leucine-sensitive hypoglycemia, ILS hypoglycemia.
leukodystrophy, melanodermic
leukopenia, severe combined immunodeficiency with
Liddle syndrome
ligand-defective apolipoprotein B-100, familial
light chain amyloidosis, immunoglobulin
light-chain deposition disease
LIH
limbs and trunk, familial lipodystrophy of lower
limit dextrinosis
LIPA deficiency
lipase D deficiency
lipase deficiency, lipoprotein
lipase deficiency, lysosomal acid
LIPD deficiency
lipid storage disease
lipid transport defect of intestine
lipidosis
lipidosis, ceramide lactoside
lipidosis, hereditary dystrophic
lipidosis, sphingomyelin
lipoatrophic diabetes
lipocalcinogranulomatosis
lipochondrodystrophy
lipodystrophy
lipodystrophy and acromegaloid gigantism, total
lipodystrophy associated with PPARG mutations, familial partial
lipodystrophy of lower limbs and trunk, familial
lipodystrophy, cephalothoracic
lipodystrophy, Dunnigan-type familial partial
lipodystrophy, Kobberling-type familial partial
lipodystrophy, reverse partial
lipodystrophy, Type 1 congenital generalized
lipodystrophy, Type 1 familial partial
lipodystrophy, Type 2 congenital generalized
lipodystrophy, Type 2 familial partial
lipodystrophy, Type 3 familial partial
lipogranulomatosis, unspecified, Farber
lipoid congenital adrenal hyperplasia
lipoid deficiency, high-density
lipoid deficiency, low-density
lipoid metabolism disorder
lipoidica, thesaurismosis
lipomatosis, benign symmetric
lipomatosis, familial benign cervical
lipomatosis, multiple symmetric
lipomucopolysaccharidosis
lipoprotein deficiency
lipoprotein deficiency, high density
lipoprotein deficiency, Tangier-type high density
lipoprotein deficiency, Type 1 high density
lipoprotein lipase deficiency
liver arginase deficiency
liver cirrhosis, pigmentary
liver glycogen synthase deficiency
liver glycogenosis, Type I X-linked
liver glycogenosis, X-linked
liver phosphorylase kinase deficiency
liver Type 0 glycogen storage disease
liver Type 0 glycogen storage disease,
LNS
long chain acyl-CoA dehydrogenase deficiency, very
loss, isolated renal magnesium
low-density lipoid deficiency
low-density-lipoid-type hyperlipoproteinemia
low-set osmoreceptor
lower limbs and trunk, familial lipodystrophy of
LPI
LPL deficiency
LTD
lyase deficiency, 3-hydroxy-3-methylglutaryl-CoA
lyase deficiency, argininosuccinate
lyase deficiency, argininosuccinic acid
lyase deficiency, HMG-CoA
lymphocytic painless thyroiditis
lymphocytic thyroiditis, chronic
lymphocytic thyroiditis, subacute
lymphoproliferative syndrome, autoimmune
lysine intolerance
lysine malabsorption syndrome
lysine metabolism disorder
lysine:alpha-ketoglutarate reductase deficiency
lysinuric protein intolerance
lysosomal acid lipase deficiency
lysosomal alpha B mannosidosis
lysosomal alpha-D-mannosidase deficiency
lysosomal beta A mannosidosis
lysosomal beta-mannosidase deficiency
lysosomal cystine transport protein defect
lysosomal protective protein deficiency
lysosomal release defect, vitamin B12
