Rare – Page 419 – CheckOrphan

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Page 419

Erythropoietic Protoporphyria

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Escher Hirt syndrome

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Escobar syndrome- type B

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Esophageal atresia

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Erythrokeratodermia variabilis- Mendes da Costa type

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Congenital disorder of glycosylation type 1C

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Dyssegmental dysplasia- Rolland-Desbuquois type

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Esophageal atresia associated anomalies

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Tropical Spastic Paraparesis

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Tropical sprue

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