cranioectodermal dysplasia CED Cranioectodermal dysplasia (CED) is a rare developmental disorder characterized by congenital skeletal and ectodermal defects associated with dysmorphic features, nephronophthisis, hepatic fibrosis and ocular anomalies (mainly retinitis pigmentosa). DOID:0050577 GARD:0000359 ICD10:Q87.5 ICD9:756.9 Levin syndrome MONDO:0009032 NCIT:C129305 OMIMPS:218330 Orphanet:1515 SCTID:254093009 Sensenbrenner syndrome UMLS:C0432235 UMLS:CN016627 UMLS:CN119432 cranioectodermal dysplasia craniosynostosis syndrome, autosomal recessive syndromic craniosynostosis short rib-polydactyly syndrome inherited renal tubular disease ectodermal dysplasia syndrome rare renal tubular disease