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Entry | Name | Description | Category | Pathway | Gene |
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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] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |