Simplifying Science
™
Loading Search Box, Please Wait ...
Descipher Site Search
Try our new low-cost Blog Generator (click logo). Free trial: 30 blog posts.
Site Browser History
☚
Hormonal, Nutritional, Metabolic, and Immune Disorders C
Site Browser History
☚
Hormonal, Nutritional, Metabolic, and Immune Disorders C
DESCIPHER HEALTH ➤
Diseases
Disease by Name
Disease by Category
Lab Tests
Tests by Name
Tests by Source
Drugs
Drugs by Generic Name
Drugs by Class
Clinical Findings
Symptoms
Signs
Home
Health
Diseases & Conditions
Permutation Index
Categories
Hormonal, Nutritional, Metabolic, and Immune Disorders
Current:
Hormonal, Nutritional, Metabolic, and Immune Disorders C
S
T
E
M
Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders C
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
C-II anapolipoproteinemia
C-II deficiency, apolipoprotein
C-III deficiency, apolipoprotein
C1 deficiency, complement
C1 Niemann-Pick disease, Type
C1-esterase inhibitor deficiency
C1-inhibitor deficiency
C1INH deficiency
C1q deficiency
C1q deficiency, complement
C1QD
C1r deficiency
C1r deficiency, complement
C1s deficiency
C1s deficiency, complement
C1SD
C2 Niemann-Pick disease, Type
C2D
C3 deficiency, complement
C3 proaccelerator deficiency
C3 proactivator deficiency
C3D
C3PA deficiency
C4 deficiency
C4 deficiency, complement
C4A deficiency
C4A deficiency, complement
C4AD
C4B deficiency
C4B deficiency, complement
C4BD
C5 deficiency, complement
C5D
C6 deficiency, complement
C6D
C7 deficiency, complement
C7D
C8 beta deficiency
C8 deficiency, complement
C8 deficiency, Type II
C8B deficiency
C8D
C8D1
C8D2
C9 deficiency, complement
C9D
Ca deficiency
Ca excess
Ca overload
cachexia, pituitary
CAH
CAH, childhood-onset
CAH, classical
CAH, nonclassical
CAH1
calcific uremic arteriolopathy
calcification 1, idiopathic basal ganglia
calcification, adult-onset idiopathic nonarteriosclerotic cerebral
calcification, childhood-onset idiopathic basal ganglia
calcification, childhood-onset idiopathic nonarteriosclerotic cerebral
calcinosi, adult-onset bilateral striopallidodentate
calcinosis
calcinosis, acquired tumoral
calcinosis, adult-onset autosomal dominant striopallidodentate
calcinosis, bilateral striopallidodentate
calcinosis, childhood-onset bilateral striopallidodentate
calcinosis, hyperphosphatemic familial tumoral
calcinosis, normophosphatemic familial tumoral
calcinosis, primary hyperphosphatemic tumoral
calcinosis, tumoral
calciphylaxis
calcium deficiency
calcium excess
calcium metabolism disorder
calcium overload
caloric malnutrition
calorie deficiency
Canale-Smith Syndrome
carbamoyl phosphate synthetase deficiency
carbamoyltransferase deficiency, ornithine
carbamyl phosphate synthetase deficiency
carbamyl phosphate synthetase deficiency, late-onset
carbamyl phosphate synthetase deficiency, neonatal-onset
carbohydrate transport and metabolism, disorder of
carbohydrate-deficient glycoprotein sydrome
carbohydrate-inducible hyperlipemia
carbonic anhydrase deficiency
carbonic anhydrase I deficiency
carbonic anhydrase II deficiency
carboxylase deficiency neonatal MCD, early-onset
carboxylase deficiency, 3-methylcrotonyl-CoA
carboxylase deficiency, juvenile-onset multiple
carboxylase deficiency, late-onset multiple
carboxylase deficiency, neonatal multiple
carboxylase deficiency, propionyl-CoA
carboxylase deficiency, pyruvate
carboxylase deficiency, Type A pyruvate
carboxylase deficiency, Type B pyruvate
carboxylase deficiency, Type C pyruvate
carboxylase deficiency, unspecified, multiple
carcinoid syndrome
cardiac glycogenosis, generalized
cardiomegalia glycogenica diffusa
cardiovasorenal syndrome
carnitine deficiency
carnitine deficiency, dietary
carnitine deficiency, myopathic
carnitine deficiency, primary
carnitine deficiency, systemic
carnitine deficiency, systemic primary
carnitine transporter deficiency, plasma-membrane
carnitine uptake defect
carnosinase deficiency
carnosinemia
carrier, erythropoietic protoporphyria
carrier, Hurler syndrome
cblA-type methylmalonic acidemia
cblA-type methylmalonic aciduria
cblA-type vitamin B12-responsive methylmalonic aciduria
cblB-type methylmalonic acidemia
cblB-type methylmalonic aciduria
cblB-type vitamin B12-responsive methylmalonic aciduria
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
cblD-type methylmalonic aciduria and homocystinura
cblE-type homocystinuria and megaloblastic anemia
cblE-type methylcobalamin deficiency
cblE-type vitamin B12-responsive homocystinuria
cblF
cblF-type methylmalonic acidemia and homocystinuria
cblF-type methylmalonic aciduria and homocystinuria
cblG-type homocystinuria and megaloblastic anemia
CBS deficiency
CDG
CDG I
CDG Ia
CDG Ib
CDGIc
CDSP
cell disease, inclusion
cell dyscrasia of unknown significance, plasma
cell dysplasia, intestinal epithelial
cell histiocytosis, Langerhans
cell histiocytosis, multifocal Langerhans
cell hyperplasia, adrenocorticotropic
cell hyperplasia, juxtaglomerular
cell hyperplasia, unspecified, islet
cell hypertrophy, juxtaglomerular
cell-mediated immunity deficiency
cellular immunodeficiency with normal immunoglobulins
central diabetes insipidus
central hyperthyroidism
central hypothyroidism
central precocious puberty, female
central precocious puberty, female idiopathic
central precocious puberty, female organic
central precocious puberty, male
CEP
cephalothoracic lipodystrophy
CEPT deficiency
ceramidase deficiency
ceramidase deficiency, acid
ceramide lactoside lipidosis
ceramide trihexosidase deficiency
ceramidosis, lactosyl
cerebral calcification, adult-onset idiopathic nonarteriosclerotic
cerebral calcification, childhood-onset idiopathic nonarteriosclerotic
cerebral Gaucher disease, adult
cerebral Gaucher disease, juvenile
cerebral Gaucher's disease, infantile
cerebral pseudosclerosis
cerebrovascular ferrocalcinosis
ceruloplasmin deficiency
cervical lipomatosis, familial benign
CF
CFB
CFDD
CFPD
CGL1
CGL2
chain acyl-CoA dehydrogenase deficiency, medium
chain acyl-CoA dehydrogenase deficiency, very long
chain amyloidosis, immunoglobulin light
chain disease, alpha heavy
chain disease, delta heavy
chain disease, gamma heavy
chain disease, mu heavy
chain disease, unspecified, heavy
cherry red spot- myoclonus syndrome
childhood hyperphosphatasemia, transient
childhood hypophosphatasia
childhood-onset bilateral striopallidodentate calcinosis
childhood-onset CAH
childhood-onset congenital adrenal hyperplasia
childhood-onset growth hormone deficiency
childhood-onset IBGC
childhood-onset idiopathic basal ganglia calcification
childhood-onset idiopathic nonarteriosclerotic cerebral calcification
chloride diarrhea, congenital secretory
chloride diarrhea, Finnish-type congenital
chloride-resistant metabolic alkalosis
chloride-responsive metabolic alkalosis
chloridorrhea, congenital
cholestais, citrin-deficiency neonatal intrahepatic
cholesterol desmolase deficiency
cholesterol ester storage disease
cholesterol ester transfer protein deficiency
cholesterol esterification block, Niemann-Pick disease with
cholesterol side-chain cleavage enzyme deficiency
cholesterol, high blood
choroid and retina, hyperornithinemia with gyrate atrophy of
chronic adrenal cortical insufficiency
chronic adrenocortical insufficiency
chronic histiocytosis X
chronic inflammation
chronic inflammatory disease
chronic isovaleric acidemia
chronic lymphocytic thyroiditis
chronic neuronopathic Gaucher disease
chronic neuronopathic Niemann-Pick disease
chronic respiratory acidosis
chronic respiratory alkalosis
chylomicron retention disease
CIDX
circulatory overload
cirrhosis with deposition of abnormal glycogen, familial
cirrhosis, bronzed
cirrhosis, pigmentary liver
citrin deficiency
citrin-deficiency neonatal intrahepatic cholestais
citrullinemia
citrullinemia, adult-onset Type II
citrullinemia, classic
citrullinemia, neonatal-onset Type II
citrullinemia, Type I
citrullinuria
classic citrullinemia
classic galactosemia
classic GnRH deficiency
classic gonadotropin releasing hormone deficiency
classic hemochromatosis
classical Bartter syndrome
classical CAH
classical congenital adrenal hyperplasia
cleavage enzyme deficiency, cholesterol side-chain
climacteric, male
CLT
CMO I deficiency
CMO II deficiency
CMRD
CoA dehydrogenase deficiency, glutaryl
CoA dehydrogenase deficiency, isovaleric acid
CoA dehydrogenase deficiency, multiple acyl
cobalamin deficiency
cobalamin F disease
cobalamin metabolism disorder
cobalamin pseudodeficiency
cobalamin R binder protein deficiency
cofactor deficiency, molybdenum
coma, diabetes with hyperosmolar
coma, diabetes with hyperosmolar nonketotic
coma, diabetic
coma, diabetic hyperglycemic hyperosmotic
coma, diabetic hypoglycemic
coma, diabetic insulin-induced
coma, myxedema
combined deficiency of methylmalonyl-CoA mutase and homocysteine:methyltetrahydrofolate methyltransferase
combined hypercholesterolemia, familial
combined hyperlipidemia
combined immunity deficiency
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, 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
combined immunodeficiency, X-linked
combined pituitary hormone deficiency 1
combined pituitary hormone deficieny 2
combined spinal cord degeneration, vitamin B12 deficiency with subacute
common variable immunodeficiency
complement C1 deficiency
complement C1q deficiency
complement C1r deficiency
complement C1s deficiency
complement C2 deficiency
complement C3 deficiency
complement C4 deficiency
complement C4A deficiency
complement C4B deficiency
complement C5 deficiency
complement C6 deficiency
complement C7 deficiency
complement C8 deficiency
complement C9 deficiency
complement component 2 deficiency
complement component 3 deficiency, autosomal recessive
complement component 5 deficiency
complement component 6 deficiency
complement component 7 deficiency
complement component 8 deficiency
complement component 8 deficiency, Type I
complement component 8 deficiency, Type II
complement component 8B deficiency
complement component 9 deficiency
complement deficiency
complement factor B deficiency
complement factor D deficiency
complement factor properdin deficiency
complete HPRT deficiency
complex deficiency, BCKD
complex deficiency, branched-chain alpha-keto dehydrogenase
complex deficiency, sarcosine dehydrogenase
component 2 deficiency, complement
component 3 deficiency, autosomal recessive complement
component 5 deficiency, complement
component 6 deficiency, complement
component 7 deficiency, complement
component 8 deficiency, complement
component 8 deficiency, Type I complement
component 8 deficiency, Type II complement
component 8B deficiency, complement
component 9 deficiency, complement
congenital adrenal hyperplasia
congenital adrenal hyperplasia 1
congenital adrenal hyperplasia, childhood-onset
congenital adrenal hyperplasia, classical
congenital adrenal hyperplasia, lipoid
congenital adrenal hypoplasia
congenital adrenal hypoplasia iwth hypogonadotropic hypogonadism
congenital aleukia
congenital chloride diarrhea, Finnish-type
congenital chloridorrhea
congenital disorder of glycosylation
congenital disorder of glycosylation, Type I
congenital disorder of glycosylation, Type Ia
congenital disorder of glycosylation, Type Ib
congenital disorder of glycosylation, Type Ic
congenital dopamine-beta-hydroxylase deficiency
congenital erythropoietic porphyria
congenital familial protracted diarrhea with enterocyte brush-border abnormalities
congenital generalized lipodystrophy, Type 1
congenital generalized lipodystrophy, Type 2
congenital hepatic porphyria
congenital hyperammonemia, Type I
congenital hyperinsulinism
congenital hypopituitarism
congenital hypothyroidism
congenital lactase deficiency
congenital malabsorptive diarrhea
congenital microvillous atrophy
congenital secretory chloride diarrhea
congenital secretory diarrhea
congenital secretory sodium diarrhea
congenital self-healing reticulohistiocytosis
congenital sodium diarrhea
congenital sucrose intolerance
congenital sucrose-isomaltose malabsorption
congenital thyroid insufficiency
congenital tufting enteropathy
congenital X-linked agammaglobulinemia
congential dystrophy, Type 1 Berardinelli-Seip
congential dystrophy, Type 2 Berardinelli-Seip
Conn's syndrome
copper deficiency
copper metabolism disorder
copper storage disease
copper transport disease
coproporphyria, erythropoietic
coproporphyria, hepatic
coproporphyria, hereditary
coproporphyria, homozygous hereditary
coproporphyrinogen oxidase deficiency
cord degeneration, vitamin B12 deficiency with subacute combined spinal
Cori disease
coritcal hyperplasia, micronodular adrenal
corneal dystrophy, dyslipoproteinemic
corneal dystrophy, keratosis palmoplantaris with
corporis diffusum universale, angiokeratoma
cortical hyperfunction, glucocorticoid-excess adrenal
cortical hyperfunction, mineralocorticoid-excess adrenal
cortical hyperplasia, adrenal
cortical hyperplasia, macronodular adrenal
cortical hypofunction, primary adrenal
cortical hypofunction, secondary adrenal
cortical hypofunction, unspecified, adrenal
cortical insufficiency, acute adrenal
cortical insufficiency, adrenal
cortical insufficiency, chronic adrenal
cortical insufficiency, primary adrenal
cortical nephrocalcinosis
cortical nephrocalcinosis, benign nodular
corticoadrenal insufficiency
corticosterone methyloxidase deficiency, Type I
corticosterone methyloxidase deficiency, Type II
corticotropin deficiency
corticotropin-releasing hormone syndrome, ectopic
CPHD1
CPHD2
CPO deficiency
CPOX deficiency
CPS deficiency
CPS I deficiency
CPX deficiency
cretinism
cretinism, athyrotic
cretinism, endemic
CRH syndrome, ectopic
Crigler-Najjar syndrome
Crigler-Najjar syndrome, Type I
Crigler-Najjar syndrome, Type II
Crigler-Najjar Type I hyperbilirubinemia
Crigler-Najjar Type II hyperbilirubinemia
crisis, acute adrenal
crisis, Addisonian
crisis, adrenal
crisis, myxedema
crisis, thyrotoxic
cryoglobulinemia
cryoglobulinemia, simple
cryoglobulinemia, Type I
cryoglobulinemia, Type II
cryoglobulinemia, Type III
CSD
CSNU
CTE
CTLN1
CTLN2
CTNS
Cu deficiency
CUA
CUD
Cushing disease
Cushing syndrome
Cushing syndrome, drug-induced
Cushing syndrome, exogenous
Cushing's disease
Cushing's syndrome
Cushing's syndrome, drug-induced
Cushing's syndrome, exogenous
Cushing's syndrome, iatrogenic
Cushing's syndrome, pituitary-dependent
cutanea tarda, porphyria
cutanea tarda, sporadic-type porphyria
cutanea tarda, Type I porphyria
cutanea tarda, Type II porphyria
cutanea tarda, Type III porphyria
cutaneous porphyria
CVID
cycle metabolism disorder, urea
CYP11A1 deficiency
CYP17A1 deficiency
CYP21 deficiency
cystathionase deficiency
cystathionine beta-synthase deficiency
cystathionine gamma-lyase deficiency
cystathionine metabolism disorder
cystathionine synthase deficiency
cystathioninuria
cystic fibrosis
cystica, osteitis fibrosa
cystine transport protein defect, lysosomal
cystinosin defect
cystinosis
cystinosis, adolescent nephropathic
cystinosis, adult nonnephropathic
cystinosis, benign nonnephropathic
cystinosis, infantile nephropathic
cystinosis, intermediate
cystinosis, late-onset juvenile nephropathic
cystinosis, nephropathic
cystinosis, ocular nonnephropathic
cystinuria
cytomegalic adrenocortical hypoplasia