Focal or diffuse thickening of the skin not inherited as a primary genetic disorder. Causes include inflammatory skin disorders, infectious disorders, lymphedema, and medications. [ NCIT:P378 ]
Synonyms: acquired keratosis keratoderma - acquired acquired keratoderma keratoderma, acquired
Term information
- SCTID:400166009 (MONDO:equivalentTo)
- UMLS:C0022581 (MONDO:equivalentTo)
- NCIT:C34746 (MONDO:equivalentTo)
- DOID:13072 (MONDO:equivalentTo)
- ICD9:701.1 (MONDO:i2s)
- MEDGEN:44016 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_integumentary_system_disorder
http://purl.obolibrary.org/obo/NCIT_C34746
http://linkedlifedata.com/resource/umls/id/C0022581
http://purl.obolibrary.org/obo/DOID_13072
http://identifiers.org/medgen/44016
http://identifiers.org/snomedct/400166009