A group of autosomal dominant, autosomal recessive, X-linked inherited or acquired disorders characterized by the thickening of the palms and soles due to hyperkeratosis. [ NCIT:C34748 ]
Synonyms: keratosis palmaris et plantaris palmoplantar keratoderma
Term information
- DOID:3390 (MONDO:equivalentTo)
- SCTID:706885006 (MONDO:equivalentTo)
- ICD9:757.39 (MONDO:relatedTo)
- NCIT:C34748 (MONDO:equivalentTo)
- EFO:1000745 (MONDO:equivalentTo)
- UMLS:C0022596 (MONDO:equivalentTo)
- MEDGEN:44017 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, mondo_top_grouping_integumentary_system_disorder, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, 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_C34748
http://identifiers.org/medgen/44017
http://identifiers.org/snomedct/706885006
http://purl.obolibrary.org/obo/DOID_3390
http://linkedlifedata.com/resource/umls/id/C0022596
http://www.ebi.ac.uk/efo/EFO_1000745