Rare – Page 492 – CheckOrphan

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Kallikrein hypertension

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Polycystic ovarian disease- familial

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Polycystic ovaries urethral sphincter dysfunction

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Kaplan Plauchu Fitch syndrome

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Kaplowitz Bodurtha syndrome

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Chromosome 8- partial trisomy

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Glycogen storage disease type 6

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Glycogen storage disease type 6- due to phosphorylation

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Polycystic kidney disease- type 2

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Polycystic kidneys- severe infantile with tuberous sclerosis

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