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Entry Name Description Category Pathway Gene
H00766 Wolcott-Rallison syndrome Wolcott-Rallison syndrome is a rare autosomal recessive disorder characterized by neonatal insulin-requiring diabetes and associated with skeletal dysplasia and growth retardation. Diabetes appears during ... Endocrine and metabolic disease EIF2AK3 [HSA:9451] [KO:K08860]
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