Oculo-ectodermal syndrome (OES) is characterized by the association of epibulbar dermoids and aplasia cutis congenital. [ Orphanet:3339 ]
Synonyms: aplasia cutis congenita-epibulbar dermoids syndrome oculoectodermal syndrome, somatic oculoectodermal syndrome
Term information
- DOID:0111705 (MONDO:equivalentTo)
- Orphanet:3339 (OMIM:600268)
- GARD:10366 (MONDO:GARD)
- icd11.foundation:1983176633 (MONDO:equivalentTo)
- OMIM:600268 (Orphanet:3339/e)
- SCTID:723554006 (MONDO:equivalentTo)
- UMLS:C1838329 (MONDO:equivalentTo)
- MESH:C563969 (MONDO:equivalentTo)
- MEDGEN:333068 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, ordo_disorder, gard_rare, mondo_top_grouping_integumentary_system_disorder, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_included, nord_rare, rare, orphanet_rare, harrisons_view_integumentary_system_disorder, mondo_top_grouping_syndromic_disease, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, ordo_malformation_syndrome, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease
http://identifiers.org/mesh/C563969
http://purl.obolibrary.org/obo/DOID_0111705
http://linkedlifedata.com/resource/umls/id/C1838329
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1983176633
http://identifiers.org/snomedct/723554006
http://www.orpha.net/ORDO/Orphanet_3339
https://omim.org/entry/600268
http://identifiers.org/medgen/333068
oculo-ectodermal syndrome
aplasia cutis congenita with epibulbar dermoids
Toriello Lacassie Droste syndrome
oes