Rare – Page 498 – CheckOrphan

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Stickler syndrome- type 3

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Stiff skin syndrome

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Multiple sulfatase deficiency

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Multiple sclerosis ichthyosis factor 8 deficiency

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Cardiomyopathy hearing loss type t RNA lysine gene mutation

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Cardiomyopathy due to anthracyclines

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Cardiogenital syndrome

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Cardiofaciocutaneous syndrome

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Cardiomyopathy cataract hip spine disease

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Cardiomelic syndrome Stratton Koehler type

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