Related MeSH Hierarchy (5)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Polycystic Kidney Diseases
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Ciliopathies » Polycystic Kidney Diseases
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Kidney Diseases, Cystic » Polycystic Kidney Diseases
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Kidney Diseases, Cystic » Polycystic Kidney Diseases
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Kidney Diseases, Cystic » Polycystic Kidney Diseases
Description
Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. MeSH
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Subtype Terms (2)
Polycystic Kidney, Autosomal Dominant
30 drugs (14 approved, 16 experimental)
Polycystic Kidney, Autosomal Recessive
2 drugs (1 approved, 1 experimental)
Phase 2 Indicated Drugs (3)
Phase 1 Indicated Drugs (1)
Other Experimental Indicated Drugs (2)
Organization Involved with Phase 4 Indications (7)
Organization Involved with Phase 3 Indications (32)
Organization Involved with Phase 2 Indications (13)
Organization Involved with Phase 1 Indications (3)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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