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CYP11B1
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Body Atlas
Most Correlated Tissues
Adrenal gland cortex
Adrenal gland
Lymph nodes
Myeloid cells of peripheral blood
Eosinophil of peripheral blood
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Disease Atlas
Most Correlated Diseases
Congenital adrenal hyperplasia
Disorder of adrenal gland
Adrenal cancer
Alpha-1-antitrypsin deficiency
11p partial monosomy syndrome
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Mitotane
nifenazone
2-ethylhexanol
Thalidomide
EDIL3 protein, human
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Most Correlated Gene Perturbations
mrp2
TUBB6
CLCN2
HOTAIRM1
ZNF365
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Literature
Most Relevant Literature
Identification and functional characterization of compound heterozygous CYP11B1 gene mutations.
Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylas…
Aldosterone synthase inhibition in humans.
Unequal crossing over between CYP11B2 and CYP11B1 causes 11 β -hydroxylase deficiency in a consangui…
Genetic analysis of a case with 11β hydroxylase deficiency caused by CYP11B2/CYP11B1 chimeric gene].
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Clinical Trials
Most Relevant Clinical Trials
Postmortem Evaluation of Adrenal and Other Endocrine Tumors in Patients With Sudden Death
Linear Growth of Children With Congenital Adrenal Hyperplasia
Evaluation of 123I-Iodometomidate for Adrenal Scintigraphy
Unilateral Primary Aldosteronism, Mineralocorticoid Antagonists Versus Surgical Treatment
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