Medicine and Dentistry
Polycystic Kidney Disease
90%
Disease
75%
Kidney Malformation
65%
Diagnosis
52%
Nephropathy
48%
Genetic Screening
46%
Prevalence
45%
Clinical Genetics
42%
PKD1
42%
Counseling
35%
Chronic Kidney Disease
31%
Urinary System
31%
Congenital Malformation
28%
Patient Registry
28%
Renal Cyst
26%
Proteinuria
24%
End Stage Renal Disease
23%
Family History
22%
Renal Agenesis
22%
Megalin
21%
Pyridoxine
21%
Hypercalciuria
21%
Patient Characteristics
21%
International Classification of Diseases
21%
Renal Glomerulus
21%
Hypophosphatasia
21%
Dent's Disease
21%
Fetus Echography
21%
Learning Disorder
21%
Mouth Pain
21%
Rokitansky Syndrome
21%
Urinary Tract Infection
21%
Second Trimester Pregnancy
20%
Urolithiasis
19%
Nephrocalcinosis
17%
Single Nucleotide Polymorphism
15%
Kidney Function
14%
Patient Care
14%
Language Delay
14%
Strabismus
14%
Family Counseling
14%
Arteriole
10%
Ligation
10%
Health Care Provider
10%
Glomerulus Filtration
10%
Glomerulus
10%
Whole Genome Sequencing
10%
Genetic Disorder
10%
Autosomal Dominant Inheritance
8%
Alport Syndrome
8%
Biochemistry, Genetics and Molecular Biology
Genetics
100%
Exome Sequencing
53%
HNF1B
53%
Prevalence
47%
Autosomal Dominant Polycystic Kidney
42%
Mosaicism
31%
Patient Registry
29%
Genomics
28%
Genetic Screening
27%
Penetrance
25%
PKD1
25%
Haploinsufficiency
21%
Oxidation Reduction Reaction
21%
Coding Region
21%
Language Development
21%
PAX2
21%
Gene Sequence
21%
FMR1
21%
Medical Genetics
21%
International Classification of Diseases
21%
Glomerulus Filtration
21%
Retinoic Acid Receptor
21%
Sodium Channel
21%
Awareness
21%
TBX1
21%
Phenotypic Heterogeneity
21%
FBN1
21%
Copy-Number Variation
21%
Nicotinamide
21%
Second Trimester Pregnancy
20%
Next Generation Sequencing
17%
Missense
15%
LHX1
14%
Single Nucleotide Polymorphism
14%
Missense Mutation
14%
Autosomal Dominant Inheritance
12%
Dideoxynucleotide Sequencing
11%
Single-Nucleotide Polymorphism
11%
ACACA
10%
Synapsin I
10%
SNP Array
10%
Enzyme
10%
DNA Binding Domain
10%
Intellectual Disability
10%
Microdeletion Syndrome
10%
Coenzyme
10%
Hypercalcaemia
10%
MUC1
10%
Heterozygosity
10%
Adenine
10%
