Biochemistry, Genetics and Molecular Biology
Genetics
100%
Hypomagnesemia
57%
Vasopressin
52%
Eicosanoid Receptor
48%
Cotransporter
39%
Autosomal Recessive Inheritance
37%
Next Generation Sequencing
32%
Exome Sequencing
31%
Genetic Screening
31%
Aquaporin 2
26%
Allele
24%
Wild Type
23%
Bartter Syndrome
22%
Single-Nucleotide Polymorphism
21%
Autosomal Dominant Inheritance
21%
Gene Linkage
20%
Genotyping
19%
Missense Mutation
18%
LMX1B
18%
Candidate Gene
18%
Intellectual Disability
16%
Arginine Vasopressin
16%
Exon
15%
Dysplasia
14%
Receptor Gene
14%
Genetic Counseling
14%
Intraflagellar Transport
14%
Cilium
13%
Cell Membrane
13%
Genetic Disorder
13%
ATPase
13%
Fibroblast
13%
Transient Receptor Potential Channels
12%
Haplotype
12%
FXYD2
12%
Deep Sequencing
12%
Mouse
11%
Body Height
11%
RNA
10%
X Chromosome
10%
Microdeletion Syndrome
10%
Proband
9%
Linkage Analysis
9%
ABCC9
9%
Mosaicism
9%
Haploinsufficiency
8%
Autosomal Recessive Disorder
8%
Base Excess
8%
Hypokalemia
8%
Amino Acids
8%
Medicine and Dentistry
Disease
79%
Nephrogenic Diabetes Insipidus
67%
Nephropathy
39%
Diagnosis
30%
Aquaporin 2
24%
Vasopressin
24%
Genetic Disorder
23%
Vasopressin V2 Receptor
23%
Ciliopathy
21%
Argipressin
20%
Chronic Kidney Disease
19%
Congenital Malformation
17%
Receptor
17%
Urinary Tract
15%
Genetic Screening
15%
Nephronophthisis
15%
Genetic Counseling
14%
Autosomal Recessive Inheritance
13%
Hypomagnesemia
13%
Collecting Duct
12%
Symptom
12%
Gitelman Syndrome
12%
Renal Failure
11%
Bartter Syndrome
10%
Nail Patella Syndrome
9%
Next Generation Sequencing
9%
Exome Sequencing
9%
Pediatrics
9%
Epileptic Seizure
9%
Case-Control Study
9%
Fibroblast
8%
Cotransporter
7%
Counseling
7%
Kidney Tubule Disorder
7%
Polycystic Kidney Disease
7%
Severe Myoclonic Epilepsy of Infancy
7%
Autosomal Dominant Inheritance
6%
Focal Segmental Glomerulosclerosis
6%
Receptor Gene
6%
Epithelial Cell
6%
Nephrocalcinosis
6%
Magnesium
6%
Magnesium Ion
6%
Emergency Medical Technician
6%
Dysplasia
5%
Clinician
5%
Glomerulus Basement Membrane
5%
Basolateral Membrane
5%
Urinary System
5%
Primary Cilium
5%
Keyphrases
Diabetes Insipidus
67%
Vasopressin V2 Receptor
23%
Kidney
18%
Arginine Vasopressin
18%
Aquaporin-2 (AQP2)
18%
Aquaporin-2 Water Channel
15%
Kidney Disease
14%
Hypomagnesemia
13%
Gitelman Syndrome
12%
V2 Receptor
11%
Arginine
10%
Vasopressin
10%
K-Cl Cotransporter
9%
Genetic Testing
9%
Whole Exome Sequencing
9%
SCN1A
9%
Diagnostic Performance
8%
Receptor Gene
7%
Urinary Tract
7%
Genetic Defects
7%
FXYD2
7%
Genetic Kidney Disease
7%
Receptor 2
7%
Chronic Kidney Disease
6%
Chronic Kidney Disease of Unknown Etiology (CKDu)
6%
Linkage Analysis
6%
Misrouting
6%
Water Channel
6%
Dravet Syndrome
6%
Hypospadias
6%
Single nucleotide Polymorphism
6%
Thiazides
6%
Next-generation Sequencing
6%
Nail-patella Syndrome
6%
Hypocalciuria
5%
Xq28
5%
Intellectual Disability
5%
Magnesium
5%
Pathophysiology
5%
Unsolicited Findings
5%
LMX1B
5%
Long Arm
5%
X Chromosome
5%
Antidiuretic Hormone
5%
Clinical Outcomes
5%
Odds Ratio
5%
