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liddle syndrome
(phenotype)
Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
CLCNKB
BSND
SCNN1B
SCNN1G
SLC12A1
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
sodium ion transmembrane transport
excretion
Epithelial sodium channel, chordates
AR_02
Epithelial sodium channel, conserved site
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Curated Studies
Most Correlated Studies
OMIM - Liddle syndrome
OMIM - Metabolic disease
OMIM - Kidney disease
Mouse Phenotypes - Kidney diseases
OMIM - Kidney diseases
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Literature
Most Relevant Literature
Clinical analysis of drug-induced Pseudo-Bartter's syndrome: a report of five cases].
Liddle's syndrome--a case report and genetic diagnostics].
Genetic basis of Bartter syndrome in Korea.
Bartter syndrome type III and congenital anomalies of the kidney and urinary tract: an antenatal pre…
A family with Liddle syndrome caused by a novel missense mutation in the PY motif of the beta-subuni…
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Clinical Trials
Most Relevant Clinical Trials
The Chinese Mutation Hotspot of ENaC Causing Liddle's Syndrome and the Association of ENaC Variation…
Clinical Study of UMOD NKCC2 Interaction on Salt-sensitivity in Hypertension
Adrenal Hyperplasia Among Young People With PCOS
The Effects of Methylphenidate and Non-invasive Brain Stimulation on Inhibitory Control in Children …
Carbamazepine in Severe Liver Disease Due to Alpha-1 Antitrypsin Deficiency
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