autosomal dominant disease EEC syndrome DC:0000689 DOID:0060782 EEC syndrome is a genetic developmental disorder characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip/palate). GARD:0002076 ICD10:Q82.4 MESH:C536189 MONDO:0010004 NCIT:C148261 OMIM:268650 Orphanet:1896 RUDIGER syndrome Rudiger syndrome 1 SCTID:39788007 UMLS:C0406704 UMLS:CN776907 Walker-Clodius syndrome ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome ectrodactyly-cleft lip/palate syndrome ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome ectrodactyly-ectodermal dysplasia-cleft syndrome ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome ectrodactyly-ectodermal dysplasia-clefting syndrome https://rarediseases.info.nih.gov/diseases/2076/eec-syndrome syndrome or malformation associated with head and neck malformations syndromic urogenital tract malformation syndrome with limb reduction defects dysostosis of genetic origin with limb anomaly as a major feature genetic otorhinolaryngologic disease syndromic renal or urinary tract malformation secondary entropion EEC syndrome and related syndrome