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Hormonal, Nutritional, Metabolic, and Immune Disorders H
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Hormonal, Nutritional, Metabolic, and Immune Disorders H
DESCIPHER HEALTH ➤
Diseases
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Hormonal, Nutritional, Metabolic, and Immune Disorders
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Hormonal, Nutritional, Metabolic, and Immune Disorders H
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Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders H
Name Permutations by Letter
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SORT ORDER:
Name
Category
18-hydroxylase deficiency
18-hydroxylase deficiency, steroid
21-hydroxylase deficiency
21-hydroxylase deficiency, late-onset
21-hydroxylase deficiency, salt-wasting
21-hydroxylase deficiency, simple virilizing
25-hydroxyvitamin D3 deficiency, selective
3-Hydroxy-3-methylglutaric aciduria
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
4-hydroxy-L-proline oxidase deficiency
4-hydroxyphenylpyruvate dioxygenase deficiency
4-hydroxyphenylpyruvic acid oxidase deficiency
HAE
hair disease, kinky
hair disease, Menke's kinky
hair disease, steely
hair syndrome, kinky
hair syndrome, steely
HAL deficiency
HALP 1
HALP 2
Hand-Schueller-Christian disease
HANE
Hanhart dwarfism
haptoglobin deficiency
harderoporphyria
HARPO
Hartnup disease
Hartnup disorder
Hashimoto's thyroiditis
Hashimoto-Pritzker disease
Hashimoto-Pritzker syndrome
HBLRCN1
HBLRCN2
HBLRDJ
HBLRG
HBLRR
HCA1
HCA2
HCP
HDL deficiency, familial
HDLD
HDLDT1
heavy chain disease
heavy chain disease, alpha
heavy chain disease, delta
heavy chain disease, gamma
heavy chain disease, mu
hematopoietic hypoplasia, generalized
heme synthetase deficiency
hemochromatosis
hemochromatosis, autosomal dominant
hemochromatosis, classic
hemochromatosis, hereditary
hemochromatosis, juvenile
hemochromatosis, neonatal
hemochromatosis, Type 2
hemochromatosis, Type 3
hemochromatosis, Type 4
hemorrhage, adrenal
hemosiderosis
HEP
heparan sulfate sulfatase deficiency
heparan-alpha-glucosaminide N-acetlytransferase deficiency
hepatic AGT deficiency
hepatic coproporphyria
hepatic fructokinase deficiency
hepatic glycogen phosphorylase deficiency
hepatic glycogen synthase deficiency
hepatic phosphorylase kinase deficiency
hepatic porphyria, acute
hepatic porphyria, congenital
hepatocutaneous-type porphyria
hepatoerythropoietic porphyria
hepatolenticular degeneration syndrome
hepatorenal dysfunction, tyrosinemia with
hepatorenal glycogen storage disease
hepatorenal glycogenois
hepatorenal-type tyrosinosis
hereditaria, thesaurismosis
hereditary alactasia
hereditary alkaptonuria
hereditary amyloidosis, transthyretin-related
hereditary angioedema
hereditary angioneurotic edema
hereditary coproporphyria
hereditary coproporphyria, homozygous
hereditary dystrophic lipidosis
hereditary fructose intolerance
hereditary fructosuria
hereditary hemochromatosis
hereditary hyperammonemia
hereditary hypertyrosinemia, Type I
hereditary hypophosphatemic rickets with hypercalciuria
hereditary orotic aciduria
hereditary osteodystrophy, Albright
hereditary vitamin D-resistant rickets
Hers disease
heterozygous autosomal dominant hypercholesterolemia
HFE
HFE2
HFE3
HFE4
HFTC
HGPS
HGSNAT deficiency
HH
HHA
HHF1
HHF2
HHF3
HHF4
HHF5
HHF6
HHF7
HHH
HHH syndrome
HHHS
HHRH
HHS
high blood cholesterol
high density lipoprotein deficiency
high density lipoprotein deficiency, Tangier-type
high density lipoprotein deficiency, Type 1
high-anion-gap metabolic acidosis
high-density lipoid deficiency
HIGM1
HIGM2
HIGM3
HIGM4
HIGM5
HIS deficiency
histidase deficiency
histidine ammonia-lyase deficiency
histidine metabolism disorder
histidinemia
histiocytosis X
histiocytosis X, chronic
histiocytosis, Langerhans cell
histiocytosis, multifocal Langerhans cell
HL deficiency
HLCS deficiency
HMG-CoA lyase deficiency
HMGCL deficiency
HND
HOGA
holocarboxylase synthetase deficiency
HOMG1
HOMG2
HOMG3
HOMG4
HOMG5
HOMG6
homocysteine:methyltetrahydrofolate methyltransferase, combined deficiency of methylmalonyl-CoA mutase and
homocystinura, cblD-type methylmalonic aciduria and
homocystinuria
homocystinuria and megaloblastic anemia, cblE-type
homocystinuria and megaloblastic anemia, cblG-type
homocystinuria, cblC-type methylmalonic acidemia and
homocystinuria, cblC-type methylmalonic aciduria and
homocystinuria, cblC-type vitamin B12-responsive methylmalonic aciduria and
homocystinuria, cblD-type methylmalonic acidemia and
homocystinuria, cblE-type vitamin B12-responsive
homocystinuria, cblF-type methylmalonic acidemia and
homocystinuria, cblF-type methylmalonic aciduria and
homogentisate 1-2-dioxygenase deficiency
homogentisic acid oxidase deficiency
homogentisic aciduria
homozygous autosomal dominant hypercholesterolemia
homozygous hereditary coproporphyria
HOPS
hormone deficiency 1, combined pituitary
hormone deficiency with hypogammaglobulinemia, growth
hormone deficiency, adrenocorticotropic
hormone deficiency, adult-onset gonadotropin releasing
hormone deficiency, adult-onset growth
hormone deficiency, autosomal dominant isolated growth
hormone deficiency, autosomal recessive isolated growth
hormone deficiency, childhood-onset growth
hormone deficiency, classic gonadotropin releasing
hormone deficiency, growth
hormone deficiency, Type IA isolated growth
hormone deficiency, Type IB isolated growth
hormone deficiency, Type II isolated growth
hormone deficiency, Type III isolated growth
hormone deficiency, X-linked agammaglobulinemia and isolated growth
hormone deficiency, X-linked hypogammaglobulinemia and isolated growth
hormone deficieny 2, combined pituitary
hormone excess, thyroid-stimulating
hormone insensitivity syndrome, growth
hormone overproduction, growth
hormone overproduction, thyroid-stimulating
hormone receptor deficiency, growth
hormone resistance, adult thyroid
hormone resistance, generalized autosomal dominant thyroid
hormone resistance, generalized autosomal recessive thyroid
hormone resistance, prepubertal thyroid
hormone resistance, selective pituitary thyroid
hormone secretion, ectopic
hormone secretion, ectopic antidiuretic
hormone syndrome, ectopic corticotropin-releasing
hormone unresponsiveness, autosomal dominant thyroid
hormone unresponsiveness, autosomal recessive thyroid
hormone, inappropriate secretion of antidiuretic
hormone, pituitary resistance to thyroid
hormone, syndrome of inappropriate secretion of antidiuretic
hormone-induced hypopituitarism
HP1
HP2
HP3
HPDR
HPP
HPPA
HPPC
HPPI
HPPO
HPRT deficiency
HPRT deficiency, complete
HPRT deficiency, partial
HPRT-related gout
HPRT1 deficiency, partial
HRPT1 deficiency
HSDB
humoral immunity deficiency
Hunter syndrome
Hurler syndrome
Hurler syndrome carrier
Hurler-Scheie syndrome
Hutchinson-Gilford progeria syndrome
HVDRR
hydroxylase deficiency, phenylalanine
hydroxylase deficiency, tyrosine
hydroxylation-deficient rickets, Type 1A vitamin D
hydroxylation-deficient rickets, Type 1B vitamin D
hydroxylysinuria
hydroxymethylglutaric aciduria
hydroxyprolinemia
hydroxypyruvate reductase deficiency, glyoxylate reductase and
HYP
hyper-beta-alaninemia
hyper-beta-aminoisobutyric aciduria
hyper-IgM immunodeficiency, autosomal recessive
hyper-IgM immunodeficiency, X-linked
hyper-IgM syndrome
hyper-IgM syndrome 1
hyper-IgM syndrome 2
hyper-IgM syndrome 3
hyper-IgM syndrome 4
hyper-IgM syndrome 5
hyper-IgM, Type 1 immunodeficiency with
hyper-IgM, Type 2 immunodeficiency with
hyper-IgM, Type 3 immunodeficiency with
hyper-IgM, Type 4 immunodeficiency with
hyper-IgM, Type 5 immunodeficiency with
hyper-IgM, unspecified, immunodeficiency with
hyperalaninemia
hyperaldosteronism
hyperaldosteronism syndrome, ACTH-dependent
hyperaldosteronism, glucocorticoid-suppressible
hyperaldosteronism, hyperreninemic
hyperaldosteronism, normotensive secondary
hyperaldosteronism, Type I familial
hyperaldosteronism, Type II familial
hyperalphalipoproteinemia
hyperalphalipoproteinemia 1
hyperalphalipoproteinemia 2
hyperammonemia, hereditary
hyperammonemia, Type I congenital
hyperandrogenism, adrenal
hyperandrogenism, ovarian
hyperapolipoproteinemia
hyperargininemia
hyperbetalipoproteinemia
hyperbetalipoproteinemia with prebetalipoproteinemia
hyperbilirubinemia I
hyperbilirubinemia II
hyperbilirubinemia, Arias-type
hyperbilirubinemia, Crigler-Najjar Type I
hyperbilirubinemia, Crigler-Najjar Type II
hyperbilirubinemia, Dubin-Johnson type
hyperbilirubinemia, Gilbert-type
hyperbilirubinemia, primary shunt
hyperbilirubinemia, Rotor-type
hypercalcemia
hypercalcemia 1, familial benign
hypercalcemia 2, familial benign
hypercalcemia with nephrocalcinosis and indicanuria, familial
hypercalcemia, acquired hypocalciuric
hypercalcemia, familial benign
hypercalcemia, Type I familial hypocalciuric
hypercalcemia, Type II familial hypocalciuric
hypercalcemic nephropathy
hypercalciuria
hypercalciuria 1, absorptive
hypercalciuria 2, absorptive
hypercalciuria, hereditary hypophosphatemic rickets with
hypercalciuria, idiopathic
hypercalciuric rickets
hyperchloremic acidosis
hyperchloremic metabolic acidosis
hypercholesterolemia
hypercholesterolemia with endogenous hyperglyceridemia
hypercholesterolemia, autosomal dominant
hypercholesterolemia, familial
hypercholesterolemia, familial combined
hypercholesterolemia, heterozygous autosomal dominant
hypercholesterolemia, homozygous autosomal dominant
hypercholesterolemia, Type B autosomal dominant
hyperchylomicronemia
hyperchylomicronemia, familial
hypercorticism
hypercortisolism
hyperdibasic aminoaciduria
hyperestrogenism, ovarian
hyperfunction, adrenal medullary
hyperfunction, glucocorticoid-excess adrenal cortical
hyperfunction, iatrogenic ovarian
hyperfunction, medulloadrenal
hyperfunction, mineralocorticoid-excess adrenal cortical
hyperfunction, unspecified, ovarian
hyperfunction, unspecified, testicular
hypergammaglobulinemia
hypergammaglobulinemia, polyclonal
hyperglycemic hyperosmotic coma, diabetic
hyperglyceridemia
hyperglyceridemia, hypercholesterolemia with endogenous
hyperglycerolemia
hyperglycinemia, ketotic
hyperglycinemia, nonketotic
hyperglycinemia, transient neonatal
hyperglycinuria
hypergonadotropic ovarian failure, X-linked
hyperimidodopeptiduria
hyperimmunoglobulin M syndrome
hyperinsulinemia
hyperinsulinemic hypoglycemia 1, familial
hyperinsulinemic hypoglycemia 2, familial
hyperinsulinemic hypoglycemia 3, familial
hyperinsulinemic hypoglycemia 4, familial
hyperinsulinemic hypoglycemia 5, familial
hyperinsulinemic hypoglycemia 6, familial
hyperinsulinemic hypoglycemia 7, familial
hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
hyperinsulinemic hypoglycemia of infancy
hyperinsulinemic hypoglycemia of infancy, persistent
hyperinsulinemic hypoglycemia, adult persistent
hyperinsulinemic hypoglycemia, exercise-induced
hyperinsulinemic hypoglycemia, persistent
hyperinsulinism with pancreatic nesidioblastosis, familial
hyperinsulinism, congenital
hyperinsulinism-hyperammonemia syndrome
hyperkalemia
hyperkalemia, familial hypertensive
hyperkalemia-hypertension syndrome, Gordon
hyperkalemic normal-anion-gap metabolic acidosis
hyperlipemia, Burger-Grutz-type idiopathic
hyperlipemia, carbohydrate-inducible
hyperlipemia, essential familial
hyperlipidemia
hyperlipidemia, combined
hyperlipidemia, Group A
hyperlipidemia, Group B
hyperlipidemia, unspecified, mixed
hyperlipoproteinemia
hyperlipoproteinemia VLDL hyperlipoproteinemia, very-low-density-lipoid-type
hyperlipoproteinemia, LDL
hyperlipoproteinemia, low-density-lipoid-type
hyperlipoproteinemia, Type I
hyperlipoproteinemia, Type Ia
hyperlipoproteinemia, Type Ib
hyperlipoproteinemia, Type IIa
hyperlipoproteinemia, Type IIb
hyperlipoproteinemia, Type III
hyperlipoproteinemia, Type IV
hyperlipoproteinemia, Type V
hyperlipoproteinemia, very-low-density-lipoid-type hyperlipoproteinemia VLDL
hyperlysinemia
hypermagnesemia
hypermethioninemia, isolated persistent
hypernatremia
hypernatremia, essential
hypernatremia, hypersmolality or
hyperornithinemia with gyrate atrophy of choroid and retina
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
hyperosmolality, diabetes with
hyperosmolar coma, diabetes with
hyperosmolar nonketotic coma, diabetes with
hyperosmotic coma, diabetic hyperglycemic
hyperostosis-hyperphosphatemia syndrome
hyperoxaluria, Type I primary
hyperoxaluria, Type II primary
hyperoxaluria, Type III primary
hyperoxaluria, unspecified, primary
hyperparathyroidism
hyperparathyroidism, primary
hyperphenylalaninemia
hyperphenylalaninemia C, BH4-deficient
hyperphosphatasemia, benign familial
hyperphosphatasemia, familial
hyperphosphatasemia, transient
hyperphosphatasemia, transient childhood
hyperphosphatemia, familial intermittent
hyperphosphatemia, infantile
hyperphosphatemic familial tumoral calcinosis
hyperphosphatemic tumoral calcinosis, primary
hyperplasia 1, congenital adrenal
hyperplasia I, adrenal
hyperplasia II, adrenal
hyperplasia III, adrenal
hyperplasia IV, adrenal
hyperplasia V, adrenal
hyperplasia, adrenal
hyperplasia, adrenal cortical
hyperplasia, adrenal medullary
hyperplasia, adrenocorticotropic cell
hyperplasia, childhood-onset congenital adrenal
hyperplasia, classical congenital adrenal
hyperplasia, congenital adrenal
hyperplasia, hyperinsulinemic hypoglycemia due to focal adenomatous
hyperplasia, hypertensive adrenal
hyperplasia, juxtaglomerular cell
hyperplasia, lipoid congenital adrenal
hyperplasia, macronodular adrenal cortical
hyperplasia, micronodular adrenal coritcal
hyperplasia, nonclassical adrenal
hyperplasia, primary thyroid
hyperplasia, secondary thyroid
hyperplasia, unspecified, islet cell
hyperplastic goiter
hyperpotassemia
hyperpotassemia and hypertension, familial
hyperprebetalipoproteinemia
hyperprolactinemia
hyperprolinemia
hyperprolinemia, Type A
hyperprolinemia, Type B
hyperprolinemia, Type I
hyperprolinemia, Type II
hyperprostaglandin E syndrome
hyperreninemic hyperaldosteronism
hyperreninemic hypoaldosteronism 1A, familial
hyperreninemic hypoaldosteronism 1B, familial
hyperreninism
hypersarcosinemia
hypersmolality
hypersmolality or hypernatremia
hyperstimulation syndrome, ovarian
hypertension, familial hyperpotassemia and
hypertensive adrenal hyperplasia
hypertensive hyperkalemia, familial
hyperthecosis, ovarian
hyperthyroidism
hyperthyroidism, adenomatous goiter with
hyperthyroidism, central
hyperthyroidism, familial
hyperthyroidism, iodine-induced
hyperthyroidism, nodular goiter with
hyperthyroidism, struma nodosa with
hyperthyroxinemia, familial euthyroid
hypertonic dehydration
hypertransferritinemia-cataract syndrome
hypertriglyceridemia
hypertriglyceridemia, familial
hypertriglyceridemia, pure
hypertrophy, juxtaglomerular cell
hypertryptophanemia, familial
hypertyrosinemia, Type I hereditary
hyperuricemia
hypervallinemia
hypervitaminosis A
hypervitaminosis B6
hypervitaminosis D
hypervolemic hyponatremia
hypoadrenocorticism with hypoparathyroidism and superficial moniliasis
hypoadrenocorticism, familial
hypoalbuminemic protein-energy malnutrition
hypoaldosteronism
hypoaldosteronism 1A, familial hyperreninemic
hypoaldosteronism 1B, familial hyperreninemic
hypoaldosteronism with renal insufficiency, hyporeninemic
hypoaldosteronism, transient neonatal
hypoalphalipoproteinemia, familial
hypoalphalipoproteinemia, primary
hypobetalipoproteinemia
hypocalcemia
hypocalcemia, hypomagnesemia with secondary
hypocalcemic vitamin D-resistant rickets
hypocalciuric hypercalcemia, acquired
hypocalciuric hypercalcemia, Type I familial
hypocalciuric hypercalcemia, Type II familial
hypochloremic alkalosis
hypochloremic metabolic alkalosis
hypocholesterolemia
hypodipsia
hypofunction, adrenal medullary
hypofunction, anterior pituitary
hypofunction, medulloadrenal
hypofunction, posterior pituitary
hypofunction, primary adrenal cortical
hypofunction, renin-angiotensin-aldosterone system
hypofunction, secondary adrenal cortical
hypofunction, unspecified, adrenal cortical
hypofunction, unspecified, ovarian
hypofunction, unspecified, testicular
hypogammaglobulinemia
hypogammaglobulinemia and isolated growth hormone deficiency, X-linked
hypogammaglobulinemia of infancy, transient
hypogammaglobulinemia, acquired
hypogammaglobulinemia, growth hormone deficiency with
hypogammaglobulinemia, late-onset
hypoglycemia
hypoglycemia 1, familial hyperinsulinemic
hypoglycemia 2, familial hyperinsulinemic
hypoglycemia 3, familial hyperinsulinemic
hypoglycemia 4, familial hyperinsulinemic
hypoglycemia 5, familial hyperinsulinemic
hypoglycemia 6, familial hyperinsulinemic
hypoglycemia 7, familial hyperinsulinemic
hypoglycemia due to focal adenomatous hyperplasia, hyperinsulinemic
hypoglycemia of infancy, hyperinsulinemic
hypoglycemia of infancy, persistent hyperinsulinemic
hypoglycemia, adult persistent hyperinsulinemic
hypoglycemia, exercise-induced hyperinsulinemic
hypoglycemia, fasting
hypoglycemia, idiopathic ketotic
hypoglycemia, idiopathic leucine-sensitive
hypoglycemia, ILS hypoglycemia. leucine-sensitive
hypoglycemia, leucine-induced
hypoglycemia, persistent hyperinsulinemic
hypoglycemia, reactive
hypoglycemia, spontaneous
hypoglycemic coma, diabetic
hypogonadism and anosmia, hypogonadotripic
hypogonadism, adult-onset idiopathic hypogonadotropic
hypogonadism, age-associated
hypogonadism, anosmic
hypogonadism, ateliotic dwarfism with
hypogonadism, congenital adrenal hypoplasia iwth hypogonadotropic
hypogonadism, hypogonadotropic
hypogonadism, idiopathic hypogonadotropic
hypogonadism, isolated hypogonadotropic
hypogonadism, juvenile
hypogonadism, primary male
hypogonadism, testicular
hypogonadotripic hypogonadism and anosmia
hypogonadotropic hypogonadism
hypogonadotropic hypogonadism, adult-onset idiopathic
hypogonadotropic hypogonadism, congenital adrenal hypoplasia iwth
hypogonadotropic hypogonadism, idiopathic
hypogonadotropic hypogonadism, isolated
hypohaptoglobinemia
hypokalemia
hypokalemic normal-anion-gap metabolic acidosis
hypolactasia, adult-type
hypomagnesemia
hypomagnesemia 1, intestinal
hypomagnesemia 2, renal
hypomagnesemia 3, renal
hypomagnesemia 4, renal
hypomagnesemia 5 with ocular involvement, renal
hypomagnesemia 6, renal
hypomagnesemia with secondary hypocalcemia
hypomagnesemia, isolated renal
hypomagnesemia, normocalciuric renal
hypomagnesemia, primary
hypomagnesemic tetany
hyponatremia
hyponatremia, euvolemic
hyponatremia, extrarenal hypovolemic
hyponatremia, factitious
hyponatremia, hypervolemic
hyponatremia, hyposmolality or
hyponatremia, hypovolemic
hyponatremia, redistributive
hyponatremia, renal hypovolemic
hyponatremia, spurious
hypoparathyroidism
hypoparathyroidism and superficial moniliasis, hypoadrenocorticism with
hypoparathyroidism, idiopathic
hypophosphatasia
hypophosphatasia, adult
hypophosphatasia, childhood
hypophosphatasia, infantile
hypophosphatasia, mild
hypophosphatemia, autosomal dominant
hypophosphatemia, primary
hypophosphatemia, X-linked
hypophosphatemic rickets with hypercalciuria, hereditary
hypophosphatemic rickets, autosomal dominant
hypophosphatemic rickets, X-linked dominant
hypophosphatemic vitamin D-resistant rickets
hypophysectomy-induced hypopituitarism
hypophysitis, inflammatory
hypopituitarism
hypopituitarism, congenital
hypopituitarism, hormone-induced
hypopituitarism, hypophysectomy-induced
hypopituitarism, iatrogenic
hypopituitarism, postablative
hypopituitarism, postpartum
hypopituitarism, radiotherapy-induced
hypoplasia iwth hypogonadotropic hypogonadism, congenital adrenal
hypoplasia, adrenal
hypoplasia, congenital adrenal
hypoplasia, cytomegalic adrenocortical
hypoplasia, generalized hematopoietic
hypoplasia, thymic
hypopotassemia
hyporeninemic hypoaldosteronism with renal insufficiency
hyposmolality
hyposmolality or hyponatremia
hypothalamic diabetes insipidus
hypothalamic infantilism-obesity
hypothyroidism
hypothyroidism, central
hypothyroidism, congenital
hypothyroidism, iodine
hypothyroidism, iodine-induced
hypothyroidism, postsurgical
hypothyroidism, primary
hypothyroidism, secondary
hypothyroidism, subclinical
hypotonic dehydration
hypotransferrinemia, familial
hypovitaminosis D
hypovolemia
hypovolemic hyponatremia
hypovolemic hyponatremia, extrarenal
hypovolemic hyponatremia, renal
hypoxanthine guanine phosphoribosyltransferase 1 deficiency
hypoxanthine guanine phosphoribosyltransferase 1 deficiency, partial