Medicine & Life Sciences
Mutation
100%
Inflammatory Bowel Diseases
91%
Genes
67%
Phenotype
55%
Meningitis
55%
T-Lymphocytes
54%
Multiple Intestinal Atresia
52%
Complement Factor H Deficiency
51%
Kingella kingae
47%
Mevalonate Kinase Deficiency
45%
Infections
45%
Cutis Laxa
44%
Lemierre Syndrome
44%
Chronic Mucocutaneous Candidiasis
44%
Severe combined immunodeficiency due to adenosine deaminase deficiency
43%
B-Lymphocytes
42%
Bruton type agammaglobulinemia
41%
SARS Virus
40%
Central Nervous System Vasculitis
40%
Erythema elevatum diutinum
39%
Genetic Testing
39%
Primary Spontaneous Pneumothorax
39%
Qa-SNARE Proteins
39%
Lichens
39%
Loss of Function Mutation
38%
Bilateral Hearing Loss
37%
Chronic Granulomatous Disease
37%
Meningococcal Infections
36%
Vaccines
35%
Severe Combined Immunodeficiency
35%
Interleukin-17
34%
Interleukin-15
34%
Pericarditis
34%
Missense Mutation
34%
Portugal
33%
Autoimmunity
33%
Burkitt Lymphoma
33%
Infliximab
32%
Sensorineural Hearing Loss
31%
Ribonucleases
30%
Ligases
30%
Mycobacterium bovis
29%
Precision Medicine
29%
Immune System Diseases
29%
Stem Cell Transplantation
28%
Hematologic Tests
28%
Genome-Wide Association Study
28%
Child
28%
Interleukin-12
28%
Agammaglobulinemia
27%