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PedAM

Pediatric Disease Annotations & Medicines




Disease skeletal dysplasia
Phenotype C0265294|metaphyseal dysplasia
Sentences 1
PubMedID- 23239615 The patient had severe growth retardation and general skeletal dysplasia compatible with spondylo-epi-metaphyseal dysplasia; however the mutation of discoidin domain receptor (ddr) 2 gene was absent.

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