Kartagener Syndrome D007619

Related MeSH Hierarchy (12)

Diseases [C] » Respiratory Tract Diseases [C08] » Bronchial Diseases » Bronchiectasis » Kartagener Syndrome

Diseases [C] » Respiratory Tract Diseases [C08] » Ciliary Motility Disorders » Kartagener Syndrome

Diseases [C] » Respiratory Tract Diseases [C08] » Respiratory System Abnormalities » Kartagener Syndrome

Diseases [C] » Otorhinolaryngologic Diseases [C09] » Ciliary Motility Disorders » Kartagener Syndrome

Diseases [C] » Cardiovascular Diseases [C14] » Cardiovascular Abnormalities » Heart Defects, Congenital » Dextrocardia » Kartagener Syndrome

Diseases [C] » Cardiovascular Diseases [C14] » Heart Diseases » Heart Defects, Congenital » Dextrocardia » Kartagener Syndrome

Description

An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.   MeSH

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Organization Involved with Phase 2 Indications (2)

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