cranioectodermal dysplasia https://www.malacards.org/card/cranioectodermal_dysplasia CED MONDO:0009032 GARD:0000359 DOID:0050577 OMIMPS:218330 cranioectodermal dysplasia NCIT:C129305 SCTID:254093009 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). Orphanet:1515 UMLS:C4551571 MEDGEN:1641011 Sensenbrenner syndrome icd11.foundation:1588881145 ICD9:756.9 craniosynostosis syndrome, autosomal recessive syndromic craniosynostosis short rib-polydactyly syndrome inherited renal tubular disease ectodermal dysplasia syndrome