Medicine & Life Sciences
Genetic Association Studies
100%
Type 2 Diabetes Mellitus
70%
Hypertelorism with esophageal abnormality and hypospadias
44%
Infantile Refsum's Disease
42%
Cherubism
40%
Canavan Disease
39%
Genes
37%
Hyperlipoproteinemia Type I
37%
Zellweger Syndrome
37%
Phenotype
35%
von Hippel-Lindau Disease
32%
Papillary Carcinoma
28%
Amyloidosis
26%
Bardet-Biedl syndrome 2
26%
Peroxisomal Biogenesis Factor 2
24%
Pigmentary Dilution
24%
Inclusion body myopathy autosomal recessive
23%
Familial type 2 Hemiplegic migraine
22%
X-Linked Opitz GBBB Syndrome
22%
UDP-N-acetylglucosamine 2-epimerase - N-acetylmannosamine kinase
22%
ribosomal protein S19
21%
Sialic Acid Storage Disease
21%
aspartoacylase
21%
Argininosuccinic Aciduria
21%
Argininosuccinate Lyase
20%
Hypoalphalipoproteinemias
19%
Laron Syndrome
19%
Sterile Alpha Motif
18%
Diamond-Blackfan Anemia
18%
Leukocytes
18%
Bardet-Biedl Syndrome
18%
Hypophosphatemic Rickets
18%
Apolipoprotein C-III
17%
Hemangioblastoma
16%
Somatotropin Receptors
16%
Cerebral Malaria
16%
Genome
15%
Sodium-Potassium-Exchanging ATPase
15%
Migraine with Aura
15%
Rhinovirus
15%
Nuclear Localization Signals
15%
Breast Neoplasms
15%
src Homology Domains
14%
Lipoprotein Lipase
14%
Calcitriol Receptors
14%
Gene Expression
14%
Muramidase
13%
Enzyme Inhibitors
13%
Apolipoprotein A-I
13%
Hypertriglyceridemia
13%
Peritoneum
13%
Myosins
12%
Intercellular Adhesion Molecule-1
12%
Transducers
12%
Nucleic Acids
11%
Intellectual Disability
11%
Vitamin D
10%
Osteoporosis
10%
Immunity
9%
Complementary DNA
9%
Cell Cycle
9%
Proteins
8%
Ligands
8%
Peptides
7%
Databases
7%
Enzymes
6%
Kidney
6%
Neoplasms
3%