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Keyphrases
Diabetes Insipidus
100%
Vasopressin V2 Receptor
41%
Aquaporin-2 (AQP2)
38%
Gitelman Syndrome
36%
Hypomagnesemia
35%
K-Cl Cotransporter
33%
Kidney Disease
30%
Kidney
30%
Arginine Vasopressin
28%
Autosomal Recessive
27%
Genetic Testing
21%
Genetic Kidney Disease
20%
Dutch
19%
Chronic Kidney Disease
19%
Urinary Tract
19%
Whole Exome Sequencing
18%
Nail-patella Syndrome
17%
Bartter Syndrome
17%
Thiazides
17%
V2 Receptor
17%
Genetic Renal Disease
17%
Vasopressin
16%
Massively Parallel Sequencing
15%
Aquaporin-2 Water Channel
14%
Exome Sequencing
14%
Gene Encoding
14%
Water Channel
13%
Magnesium
13%
Diagnostic Yield
13%
Gorlin Syndrome
13%
Hypospadias
13%
Chronic Kidney Disease of Unknown Etiology (CKDu)
13%
SCN1A
12%
FXYD2
12%
Arginine
12%
Mg(II)
12%
Genetic Counseling
12%
Missense mutation
12%
Unsolicited Findings
12%
Autosomal Dominant
11%
Pathogenic Variants
11%
Next-generation Sequencing
11%
LMX1B
11%
Epilepsy
10%
Reabsorption
10%
Linkage Analysis
10%
Patella
10%
Family Members
10%
Collecting Duct Cells
9%
Distal Convoluted Tubule
9%
Biochemistry, Genetics and Molecular Biology
Genetics
85%
Hypomagnesemia
55%
Cotransporter
40%
Autosomal Recessive Inheritance
34%
Vasopressin
33%
Exome Sequencing
31%
Genetic Screening
31%
Chromosome
29%
Magnesium
25%
Allele
25%
Genotyping
24%
Wild Type
24%
Bartter Syndrome
23%
LMX1B
22%
Autosomal Dominant Inheritance
21%
Next Generation Sequencing
21%
Single-Nucleotide Polymorphism
20%
Gene Linkage
20%
Genomics
18%
Aquaporin 2
18%
Missense Mutation
18%
Fibroblast
17%
Candidate Gene
15%
Genetic Disorder
14%
Exon
14%
Intraflagellar Transport
14%
ATPase
14%
Intellectual Disability
13%
FXYD2
13%
ABCC9
12%
Deep Sequencing
12%
Cell Membrane
12%
X Chromosome
12%
Body Height
11%
Dysplasia
11%
RNA
11%
Genetic Marker
11%
Transient Receptor Potential Channel
11%
Microdeletion Syndrome
10%
Linkage Analysis
10%
Amino Acids
10%
Arginine Vasopressin
9%
Genetic Counseling
9%
Hypokalemia
9%
Adenosine Triphosphate
9%
Chloride
9%
Haploinsufficiency
9%
Autosomal Recessive Disorder
9%
Genetic Divergence
8%
Haplotype
8%
Medicine and Dentistry
Nephrogenic Diabetes Insipidus
84%
Genetics
72%
Diseases
59%
Nephropathy
51%
Vasopressin
35%
Aquaporin 2
33%
Chronic Kidney Disease
31%
Genetic Screening
29%
Congenital Anomalies of the Kidney and Urinary Tract
26%
Vasopressin V2 Receptor
24%
Argipressin
23%
Genetic Disorder
20%
Ciliopathy
20%
Hypomagnesemia
20%
Gitelman Syndrome
18%
Etiology
18%
Receptor
18%
Autosomal Recessive Inheritance
14%
Magnesium
14%
Nephronophthisis
14%
Renal Failure
13%
Collecting Duct
13%
Genetic Counseling
13%
Next Generation Sequencing
12%
Pathogenesis
11%
Pediatrics
10%
Severe Myoclonic Epilepsy of Infancy
10%
Receptor Gene
10%
Bartter Syndrome
9%
Case-Control Study
9%
Nephron
9%
Single Nucleotide Polymorphism
9%
Epileptic Seizure
9%
Congenital Malformation
8%
Hypoplasia
8%
Kidney Tubule Disorder
8%
Urinary System
7%
Cotransporter
7%
Gorlin Syndrome
7%
Exome Sequencing
6%
Hypospadias
6%
Aplasia
6%
Hypocalciuria
6%
Developmental Delay
6%
Magnesium Ion
6%
Epilepsy
6%
Nephrocalcinosis
6%
Nephrologist
6%
Adenosine Triphosphate
6%
Epithelial Cell
5%
