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Hormonal, Nutritional, Metabolic, and Immune Disorders S
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Hormonal, Nutritional, Metabolic, and Immune Disorders S
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Hormonal, Nutritional, Metabolic, and Immune Disorders
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Hormonal, Nutritional, Metabolic, and Immune Disorders S
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Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders S
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Name
Category
2-sulfatase deficiency, iduronate
s-PCT
saccharopine dehydrogenase deficiency
saccharopinuria
salla disease
salt-wasting 21-hydroxylase deficiency
salt-wasting 3-beta-hydroxysteroid dehydrogenase deficiency
Sanfilippo syndrome
Sanfilippo syndrome A
Sanfilippo syndrome B
Sanfilippo syndrome C
Sanfilippo syndrome D
Sanfilippo syndrome, Type A
Sanfilippo syndrome, Type B
Sanfilippo syndrome, Type C
Sanfilippo syndrome, Type D
sarcosine dehydrogenase complex deficiency
sarcosinemia
SARD deficiency
SARDH deficiency
SARDHD
SCD
Scheie syndrome
Schilder disease, bronze
Schindler disease
Schindler disease, Type I
Schindler disease, Type II
Schindler disease, Type III
Schindler type neuroaxonal dystrophy
Schmidt syndrome
Schwartz-Bartter syndrome
SCID
SCID with ionizing radiation sensitivity, T- B- NK+ autosomal recessive
SCID, T- B+ NK+ autosomal recessive
SCID, T- B+ NK-
SCID, T- B+ NK- autosomal recessive
SCID, X-linked
SCIDX
sclerocystic ovarian disease
Scotian type Nieman-Pick disease, Nova
scurvy
SD
Se deficiency
secondary adrenal cortical hypofunction
secondary adrenal insufficiency
secondary aldosteronism
secondary amyloidosis
secondary hyperaldosteronism, normotensive
secondary hypocalcemia, hypomagnesemia with
secondary hypothyroidism
secondary thyroid hyperplasia
secretion of antidiuretic hormone, inappropriate
secretion of antidiuretic hormone, syndrome of inappropriate
secretion, ectopic ADH
secretion, ectopic antidiuretic hormone
secretion, ectopic hormone
secretory chloride diarrhea, congenital
secretory diarrhea, congenital
secretory sodium diarrhea, congenital
Segawa syndrome, autosomal recessive
Seip syndrome
selective 1-alpha-25-hydroxyvitamin D3 deficiency
selective 25-hydroxyvitamin D3 deficiency
selective IgA immunodeficiency
selective IgM immunodeficiency
selective pituitary thyroid hormone resistance
selective vitamin E deficiency, Friedreich-like ataxia with
selenium deficiency
self-healing reticulohistiocytosis, congenital
sella syndrome, empty
semialdehyde synthase deficiency, alpha-aminoadipic
sensitivity, severe combined immunodeficiency with ionizing radiation
sensitivity, T- B- NK+ autosomal recessive SCID with ionizing radiation
sensitivity, T- B- NK+ autosomal recessive severe combined immunodeficiency with ionizing radiation
serine:pyruvate aminotransferase deficiency
severe combined immunodeficiency
severe combined immunodeficiency with ionizing radiation sensitivity
severe combined immunodeficiency with ionizing radiation sensitivity, T- B- NK+ autosomal recessive
severe combined immunodeficiency with leukopenia
severe combined immunodeficiency, adenosine-deaminase-deficiency
severe combined immunodeficiency, late-onset adenosine-deaminase-deficiency
severe combined immunodeficiency, Nezelof-type
severe combined immunodeficiency, T- B+ NK+ autosomal recessive
severe combined immunodeficiency, T- B+ NK- autosomal recessive
severe combined immunodeficiency, T- B+ NK- X-linked
severe malnutrition
sexual ateleiotic dwarfism
sexual infantilism
Sheehan syndrome
shunt hyperbilirubinemia, primary
SI deficiency
SIADH
sialic acid storage disease
sialic acid storage disease, adult
sialic acid storage disease, infantile
sialidase deficiency
sialidosis
sialidosis, Type I
sialidosis, Type II
sialolipidosis
sialuria
sialuria, Finnish type
sialuria, infantile
SIASD
side-chain cleavage enzyme deficiency, cholesterol
siderosis, Bantu
SIDS deficiency
Siemerling-Creutzfeldt disease
significance, monoclonal gammopathy of unknown
significance, plasma cell dyscrasia of unknown
silent thyroiditis
Simmonds disease
Simmonds syndrome
simple cryoglobulinemia
simple goiter
simple virilizing 21-hydroxylase deficiency
simplex, struma nodosa
Sindh, dwarfism of
Sly syndrome
Smith-Strang disease
sodium and extracellular volume depletion
sodium deficiency
sodium diarrhea, congenital
sodium diarrhea, congenital secretory
sodium excess
sodium overload
South-African-type porphyria
sphingomyelin lipidosis
sphingomyelinase deficiency
sphingomyelinase deficiency, Niemann-Pick disease without
spinal cord degeneration, vitamin B12 deficiency with subacute combined
spitting, excessive
spontaneous hypoglycemia
sporadic-type PCT
sporadic-type porphyria cutanea tarda
spot syndrome, myoclonus-cherry red
spot- myoclonus syndrome, cherry red
spurious hyponatremia
StAR deficiency
state, female prepubertal
state, immunocompromised
state, unspecified, nutritional deficiency
steely hair disease
steely hair syndrome
Stein-Leventhal syndrome
steroid 11-beta-hydroxylase deficiency
steroid 18-hydroxylase deficiency
steroid 18-oxidase deficiency
steroid acute regulatory protein deficiency
storage disease with vertical supranuclear ophthalmoplegia, neurovisceral
storage disease XI, glycogen
storage disease, adult sialic acid
storage disease, cholesterol ester
storage disease, copper
storage disease, hepatorenal glycogen
storage disease, infantile sialic acid
storage disease, iron
storage disease, lipid
storage disease, liver Type 0 glycogen
storage disease, N-acetylneuraminic acid
storage disease, NANA
storage disease, Type I glycogen
storage disease, Type Ia glycogen
storage disease, Type Ib glycogen
storage disease, Type Ic glycogen
storage disease, Type Id glycogen
storage disease, Type II glycogen
storage disease, Type IIA glycogen
storage disease, Type IIB glycogen
storage disease, Type IIC glycogen
storage disease, Type III glycogen
storage disease, Type IIIa glycogen
storage disease, Type IIIb glycogen
storage disease, Type IIIc glycogen
storage disease, Type IV glycogen
storage disease, Type IXa1 glycogen
storage disease, Type V glycogen
storage disease, Type VI glycogen
storage disease, Type VII glycogen
storage disease, Type VIII glycogen
storage disease, Type X glycogen
storage disease, unspecified, glycogen
storage disease, unspecified, sialic acid
storage disease, vitamin B12
storm, thyroid
storm, thyrotoxic
striopallidodentate calcinosi, adult-onset bilateral
striopallidodentate calcinosis, adult-onset autosomal dominant
striopallidodentate calcinosis, bilateral
striopallidodentate calcinosis, childhood-onset bilateral
struma granulomatosa
struma nodosa
struma nodosa simplex
struma nodosa with hyperthyroidism
struma nodosa, toxic
subacute combined spinal cord degeneration, vitamin B12 deficiency with
subacute granulomatous thyroiditis
subacute juvenile Niemann-Pick disease
subacute lymphocytic thyroiditis
subacute neuronophatic Gaucher diseease
subacute nonsupporative thyroiditis
subacute thyroiditis
subacute thyroiditis, painful
subclinical hypothyroidism
sucrase-isomaltase deficiency
sucrose intolerance, congenital
sucrose-isomaltose malabsorption, congenital
sulfamidase deficiency
sulfatase deficiency, heparan sulfate
sulfatase deficiency, sulfoiduronate
sulfate sulfatase deficiency, heparan
sulfite oxidase deficiency, xanthine dehydrogenase and aldehyde oxidase and
sulfoiduronate sulfatase deficiency
sulfur-bearing amino-acid metabolism disorder
superficial moniliasis, hypoadrenocorticism with hypoparathyroidism and
suppurative thyroiditis
supranuclear ophthalmoplegia, neurovisceral storage disease with vertical
Swedish-type porphyria
Sweeley-Klionsky disease
sydrome, carbohydrate-deficient glycoprotein
symmetric lipomatosis, benign
symmetric lipomatosis, multiple
syndrome of inappropriate secretion of antidiuretic hormone
syndrome X
Syndrome, Canale-Smith
Syndrome, Goldberg
synthase deficiency, alpha-aminoadipic semialdehyde
synthase deficiency, argininosuccinate
synthase deficiency, cystathionine
synthase deficiency, hepatic glycogen
synthase deficiency, late-onset N-acetylglutamate
synthase deficiency, liver glycogen
synthase deficiency, N-acetylglutamate
synthase deficiency, neonatal-onset N-acetylglutamate
synthase deficiency, porphobilinogen
synthase deficiency, uridine monophosphate
synthase deficiency, uroporphyrinogen
synthase deficiency, uroporphyrinogen III
synthesase deficiency, UMP
synthetase deficiency, arginosuccinate
synthetase deficiency, carbamoyl phosphate
synthetase deficiency, carbamyl phosphate
synthetase deficiency, heme
synthetase deficiency, holocarboxylase
synthetase deficiency, late-onset carbamyl phosphate
synthetase deficiency, N-acetylglutamate
synthetase deficiency, neonatal-onset carbamyl phosphate
synthetase deficiency, uridine monophosphate
syrup urine disease, maple
syrup urine disease, Type III maple
system hypofunction, renin-angiotensin-aldosterone
systemic amyloidosis
systemic amyloidosis, primary
systemic carnitine deficiency
systemic nonneuropathic amyloidosis
systemic primary carnitine deficiency