White sponge nevus (WSN) is a rare and autosomal dominant genetic disease in which the oral mucosa is white or grayish, thickened, folded, and spongy. The onset is early in life, and both sexes are affected equally. Other common sites include the tongue, floor of the mouth, and alveolar mucosa. [ Orphanet:171723 ]
Synonyms: White sponge nevus of Cannon white sponge nevus of Cannon white sponge nevus hereditary mucosal leukokeratosis
Term information
- NCIT:C84760 (MONDO:equivalentTo)
- OMIMPS:193900 (https://orcid.org/0000-0002-6601-2165)
- SCTID:389203001 (MONDO:equivalentTo)
- MEDGEN:328433 (MONDO:equivalentTo)
- Orphanet:171723 (MONDO:equivalentTo)
- DOID:0050448 (MONDO:equivalentTo)
- UMLS:C1721005 (MONDO:equivalentTo)
- ICD9:528.6 (MONDO:relatedTo)
- MESH:D053529 (MONDO:equivalentTo)
- GARD:8501 (MONDO:GARD)
matrix_llm__is_cancer_other, gard_rare, ordo_disorder, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, nord_rare, matrix_included, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, orphanet_rare, harrisons_view_integumentary_system_disorder, matrix_llm__is_glucose_dysfunction_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_hereditary_disease
http://purl.obolibrary.org/obo/DOID_0050448
http://identifiers.org/snomedct/389203001
http://www.orpha.net/ORDO/Orphanet_171723
http://linkedlifedata.com/resource/umls/id/C1721005
http://identifiers.org/medgen/328433
http://purl.obolibrary.org/obo/NCIT_C84760
http://identifiers.org/mesh/D053529
https://omim.org/phenotypicSeries/PS193900