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Hormonal, Nutritional, Metabolic, and Immune Disorders F
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Hormonal, Nutritional, Metabolic, and Immune Disorders F
DESCIPHER HEALTH ➤
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Hormonal, Nutritional, Metabolic, and Immune Disorders
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Hormonal, Nutritional, Metabolic, and Immune Disorders F
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Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders F
Name Permutations by Letter
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Z
SORT ORDER:
Name
Category
F disease, cobalamin
F Niemann-Pick disease, Type
f-PCT
Fabry disease
factitious hyponatremia
factor B deficiency
factor B deficiency, complement
factor B deficiency, properdin
factor D deficiency
factor D deficiency, complement
factor deficiency, properdin P
factor I deficiency, insulin-like growth
factor properdin deficiency, complement
FAH deficiency
failure 1, premature ovarian
failure 2A, premature ovarian
failure 2B, premature ovarian
failure 3, premature ovarian
failure syndrome, reproductive autoimmune
failure, idiopathic premature ovarian
failure, postablative ovarian
failure, postablative testicular
failure, postirradiation ovarian
failure, postirradiation testicular
failure, postsurgical ovarian
failure, postsurgical testicular
failure, unspecified, iatrogenic ovarian
failure, unspecified, iatrogenic testicular
failure, unspecified, premature ovarian
failure, X-linked hypergonadotropic ovarian
failure, X-linked premature ovarian
familial alphalipoprotein deficiency
familial amyloid polyneuropathy
familial benign cervical lipomatosis
familial benign hypercalcemia
familial benign hypercalcemia 1
familial benign hypercalcemia 2
familial cirrhosis with deposition of abnormal glycogen
familial combined hypercholesterolemia
familial defective apolipoprotein B-100
familial dysbetalipoproteinemia
familial euthyroid hyperthyroxinemia
familial HDL deficiency
familial hyperaldosteronism, Type I
familial hyperaldosteronism, Type II
familial hypercalcemia with nephrocalcinosis and indicanuria
familial hypercholesterolemia
familial hyperchylomicronemia
familial 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 hyperinsulinism with pancreatic nesidioblastosis
familial hyperlipemia, essential
familial hyperphosphatasemia
familial hyperphosphatasemia, benign
familial hyperpotassemia and hypertension
familial hyperreninemic hypoaldosteronism 1A
familial hyperreninemic hypoaldosteronism 1B
familial hypertensive hyperkalemia
familial hyperthyroidism
familial hypertriglyceridemia
familial hypertryptophanemia
familial hypoadrenocorticism
familial hypoalphalipoproteinemia
familial hypocalciuric hypercalcemia, Type I
familial hypocalciuric hypercalcemia, Type II
familial hypotransferrinemia
familial iminoglycinuria
familial intermittent hyperphosphatemia
familial isolated vitamin E deficiency
familial lactose intolerance
familial ligand-defective apolipoprotein B-100
familial lipodystrophy of lower limbs and trunk
familial Mediterranean fever
familial methionine malabsorption
familial methyloxidase deficiency
familial paroxysmal polyserositis
familial partial lipodystrophy associated with PPARG mutations
familial partial lipodystrophy, Dunnigan-type
familial partial lipodystrophy, Kobberling-type
familial partial lipodystrophy, Type 1
familial partial lipodystrophy, Type 2
familial partial lipodystrophy, Type 3
familial protracted diarrhea with enterocyte brush-border abnormalities, congenital
familial recurrent polyserositis
familial renal amyloidosis
familial Teutschlaender disease
familial tumoral calcinosis, hyperphosphatemic
familial tumoral calcinosis, normophosphatemic
familial visceral amyloidosis
familial vitamin D-resistant rickets
familial-type PCT
Fanconi syndrome
Fanconi-Bickel syndrome
Fanconi-type glycogenosis
FAP
Farber disease
Farber lipogranulomatosis
fasting hypoglycemia
fatty acid oxidation disorder
FBH1
FBH2
FBP1 deficiency
FBS
FCHL
Fe deficiency
FECH deficiency
FED
female central precocious puberty
female delayed puberty
female early normal pubertal variant
female idiopathic central precocious puberty
female normal puberty
female organic central precocious puberty
female peripheral precocious puberty
female precocious puberty
female premature adrenache
female prepubertal state
female prepuberty
female puberty, normal
female puberty, precocious
female virilization
feminization syndrome, testicular
feminization, adrenal
ferrocalcinosis, cerebrovascular
ferrochelatase deficiency
fever, familial Mediterranean
fever, periodic
FH
FH I
FH II
FHA
FHC
FHD
FHH1
FHH2
FHHA1A
FHHA1B
fibrosa cystica, osteitis
fibrosa, osteitis
fibrosa, osteodystrophia
fibrosis, cystic
fibrous thyroiditis, invasive
Finnish type sialuria
Finnish-type congenital chloride diarrhea
fish-eye disease
Fleisher syndrome
floating-betalipoproteinemia
fluid deficiency
fluid imbalance
fluid intake, excessive
fluid or electrolyte or acid-base balance disorder
fluid overload
fluid overload, transfusion-induced
fluid retention
fluid volume expansion, extracellular
fluids, lack of
FMF
focal adenomatous hyperplasia, hyperinsulinemic hypoglycemia due to
folate deficiency
folic acid balance, negative
folic acid deficiency
Folling's syndrome
Forbes disease
FPL1
FPL2
FPL3
FPLD1
FPLD2
FPLD3
French PC deficiency
French pyruvate decarboxylase deficiency
Friedreich-like ataxia with selective vitamin E deficiency
Froehlich syndrome
fructokinase deficiency
fructokinase deficiency, hepatic
fructose aldolase B deficiency
fructose biphosphate aldolase B deficiency
fructose disorder
fructose intolerance
fructose intolerance, hereditary
fructose-1-6-biphosphatase deficiency
fructose-1-6-diphosphatase deficiency
fructose-1-phosphate aldolase deficiency
fructosemia
fructosemia, benign
fructosemia, essential
fructosuria, essential
fructosuria, essential benign
fructosuria, hereditary
fucosidosis
fucosidosis, Type 1
fucosidosis, Type 2
fumarylacetoacetase deficiency