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PedAM

Pediatric Disease Annotations & Medicines




Disease skeletal dysplasia
Phenotype C0011847|diabetes
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PubMedID- 21050479 Wolcott-rallison syndrome (wrs) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune insulin-requiring diabetes associated with skeletal dysplasia and growth retardation.

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