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| Term | EEC syndrome | ID (Ontology) | DOID:0060782 (Human Disease) |
| Definition | A syndrome characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate). | ||
| Also Known As | "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome" ; "ectrodactyly-ectodermal dysplasia-clefting syndrome" ; "Rudiger syndrome 1" (for all, see Synonyms field below) | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ disease | |__syndrome____________________| EEC syndrome 1 rec. |__ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 |__ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 1 rec. |
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autosomal dominant disease syndrome |
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External Crossreferences & Linkouts
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MESH:C536189 NCI:C148261 ORDO:1896 SNOMEDCT_US_2023_03_01:39788007 UMLS_CUI:C0406704 |
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