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 B
Site Browser History
☚
Hormonal, Nutritional, Metabolic, and Immune Disorders B
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 B
S
T
E
M
Disease and Condition Index for Hormonal, Nutritional, Metabolic, and Immune Disorders B
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
11-beta-hydroxylase deficiency
11-beta-hydroxylase deficiency, steroid
11-beta-hydroxysteroid dehydrogenase deficiency Type 2
1B pseudovitamin D3 deficiency rickets, Type
1B vitamin D hydroxylation-deficient rickets, Type
1B vitamin D-dependent rickets, Type
1B, familial hyperreninemic hypoaldosteronism
2B vitamin D-dependent rickets, Type
2B, premature ovarian failure
3-beta-HSD deficiency
3-beta-hydroxydehydrogenase deficiency
3-beta-hydroxysteroid dehydrogenase deficiency
3-beta-hydroxysteroid dehydrogenase deficiency, late-onset
3-beta-hydroxysteroid dehydrogenase deficiency, non-salt-wasting
3-beta-hydroxysteroid dehydrogenase deficiency, salt-wasting
8B deficiency, complement component
B+ NK+ autosomal recessive SCID, T-
B+ NK+ autosomal recessive severe combined immunodeficiency, T-
B+ NK- autosomal recessive SCID, T-
B+ NK- autosomal recessive severe combined immunodeficiency, T-
B+ NK- SCID, T-
B+ NK- X-linked severe combined immunodeficiency, T-
B- NK+ autosomal recessive SCID with ionizing radiation sensitivity, T-
B- NK+ autosomal recessive severe combined immunodeficiency with ionizing radiation sensitivity, T-
B-100, familial defective apolipoprotein
B-100, familial ligand-defective apolipoprotein
B1 deficiency, vitamin
B12 deficiency with subacute combined spinal cord degeneration, vitamin
B12 deficiency, vitamin
B12 lysosomal release defect, vitamin
B12 storage disease, vitamin
B12-binding protein deficiency, vitamin
B12-responsive homocystinuria, cblE-type vitamin
B12-responsive methylmalonic aciduria and homocystinuria, cblC-type vitamin
B12-responsive methylmalonic aciduria, cblA-type vitamin
B12-responsive methylmalonic aciduria, cblB-type vitamin
B2 deficiency, vitamin
B6 deficiency, vitamin
B6 toxicity, vitamin
B6, hypervitaminosis
Babinski-Froehlich syndrome
baby disease, Beery
BAIB aciduria
BAIB urinary excretion
balance disorder, fluid or electrolyte or acid-base
balance, negative folic acid
Bantu siderosis
Bartter syndrome
Bartter syndrome, antenatal
Bartter syndrome, classical
Bartter syndrome, neonatal
Bartter syndrome, Type I antenatal
Bartter syndrome, Type II antenatal
basal ganglia calcification 1, idiopathic
basal ganglia calcification, childhood-onset idiopathic
Basedow disease
Basedow-Graves disease
Bassen-Kornzweig syndrome
BCKD complex deficiency
Beery baby disease
benign cervical lipomatosis, familial
benign essential pentosuria
benign familial hyperphosphatasemia
benign fructosemia
benign fructosuria, essential
benign hypercalcemia 1, familial
benign hypercalcemia 2, familial
benign hypercalcemia, familial
benign monoclonal gammopathy
benign nodular cortical nephrocalcinosis
benign nonnephropathic cystinosis
benign paroxysmal peritonitis
benign PC deficiency
benign pyruvate decarboxylase deficiency
benign symmetric lipomatosis
benign thyroid disease
Berardinelli syndrome
Berardinelli-Seip congential dystrophy, Type 1
Berardinelli-Seip congential dystrophy, Type 2
beriberi
beta A mannosidosis, lysosomal
beta deficiency, C8
beta-2-microglobulin-associated amyloidosis
beta-2m amyloidosis
beta-aminoisobutyric aciduria
beta-galactosidase deficiency
beta-glucosidase deficiency, acid
beta-glucuronidase deficiency
beta-ketothiolase deficiency
beta-mannosidase deficiency
beta-mannosidase deficiency, lysosomal
beta-mannosidosis
beta-synthase deficiency, cystathionine
BH4-deficient hyperphenylalaninemia C
bilateral striopallidodentate calcinosi, adult-onset
bilateral striopallidodentate calcinosis
bilateral striopallidodentate calcinosis, childhood-onset
bilirubin excretion disorder
binder protein deficiency, cobalamin R
biotin deficiency
biotinidase deficiency
biphosphate aldolase B deficiency, fructose
bisalbuminemia
block, Niemann-Pick disease with cholesterol esterification
blood cholesterol, high
blue diaper syndrome
bone, von Rechlinghausen's disease of
brain disease, marble
branched-chain alpha-keto dehydrogenase complex deficiency
branched-chain amino acid metabolism disturbance
branched-chain ketoaciduria
brancher deficiency
branching enzyme deficiency, glycogen
broad-betalipoproteinemia
bronze Schilder disease
bronzed cirrhosis
bronzed disease
brown tumor
Brunzell syndrome, AGPAT2-related
Brunzell syndrome, BSCL2-related
brush-border abnormalities, congenital familial protracted diarrhea with enterocyte
Bruton's disease
Bruton's-type agammaglobulinemia
BSCL1
BSCL2
BSCL2-related Brunzell syndrome
BSPDC
BTD deficiency
Buerger-Gruetz syndrome
Burger-Grutz-type idiopathic hyperlipemia