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cutis laxa
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
ATP7A
FBLN5
LOX
RIN2
LTBP1
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Pathway Enrichment
Most Correlated Biogroups
collagen-containing extracellular matrix
Complement Clr-like EGF domain
elastic fiber
extracellular matrix structural constituent
NABA_ECM_GLYCOPROTEINS
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Metabolic disease
OMIM - Cutis laxa
OMIM - Congenital disorder
OMIM - Skeletal and Integument Related Disorders
OMIM - Occipital horn syndrome
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Literature
Most Relevant Literature
Autosomal recessive cutis laxa type IIIA: Report of a patient with severe phenotype and review of th…
Cutis laxa: A comprehensive overview of clinical characteristics and pathophysiology.
Autosomal dominant cutis laxa and critical stenosis of the left main coronary artery in a 21-year-ol…
Acquired cutis laxa type II (Marshall syndrome) in a 3-month-old boy.
Autosomal recessive cutis laxa type 1C with a homozygous LTBP4 splicing variant: a case report and u…
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Clinical Trials
Most Relevant Clinical Trials
Therapy of Scars and Cutis Laxa With Autologous Adipose Derived Mesenchymal Stem Cells
Structural Analysis of Human Tissue
Use of 2-octyl-cyanoacrylate Together With a Self-adhering Mesh
Pathogenetic Basis of Aortopathy and Aortic Valve Disease
Closed Incision Disposable Negative Pressure Wound Therapy in Immediate Postmastectomy Breast Recons…
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