Ignet

Gene symbol: SDU

Gene name: skeletal dysplasia (unspecified)

HGNC ID: 10692

Related Genes

#	Gene Symbol	Number of hits
1	EIF2AK3	1 hits

Related Sentences

#	PMID	Sentence
1	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.