• UMLS:C4011926 (MONDO:equivalentTo)
• OMIM:193900 (MONDO:equivalentTo)
• DOID:0081287 (MONDO:equivalentTo)
• MEDGEN:860363 (MONDO:equivalentTo)

gard_rare, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_integumentary_system_disorder, mondo_top_grouping_member, matrix_llm__medical_specialization_member, matrix_llm__tag_existing_treatment_false, matrix_llm__is_glucose_dysfunction_false, nord_rare, matrix_included, matrix_llm__is_glucose_dysfunction_member, matrix_llm__tag_qaly_lost_low, mondo_top_grouping_cancer_or_benign_tumor, matrix_llm__is_pathogen_caused_false, matrix_txgnn_grouping_member, rare, matrix_llm__tag_qaly_lost_member, matrix_llm__anatomical_skin_disorder, harrisons_view_integumentary_system_disorder, otar, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__is_cancer_false, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_member, matrix_llm__txgnn_neurocutaneous_disease, matrix_llm__txgnn_tumor, matrix_llm__medical_specialization_dermatology, matrix_llm__txgnn_skin_condition, matrix_llm__is_pathogen_caused_member, matrix_llm__txgnn_member, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, matrix_llm__medical_specialization_genetics_and_genomics, matrix_llm__is_cancer_member, matrix_llm__anatomical_member

• hereditary mucosal leukokeratosis and has material basis in germline mutation in some KRT4

• hereditary mucosal leukokeratosis
• has material basis in germline mutation in some KRT4