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[X] hereditary palmoplantar keratoderma

Go to external page http://purl.obolibrary.org/obo/MONDO_0019272

An instance of palmoplantar keratosis that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: hereditary keratosis palmoplantaris hereditary palmoplantar keratosis hereditary PPK hereditary palmoplantar hyperkeratosis

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:590657 (MONDO:equivalentTo)
  • icd11.foundation:1941547119 (https://orcid.org/0000-0001-5208-3432)
  • SCTID:239066003 (MONDO:equivalentTo)
  • UMLS:C0406757 (MONDO:equivalentTo)
  • GARD:18988 (MONDO:GARD)
  • ICD9:757.39 (MONDO:relatedTo)
  • Orphanet:79357 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, harrisons_view_disorder_of_development_or_morphogenesis, disease_grouping, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_integumentary_system_disorder, mondo_top_grouping_member, matrix_llm__txgnn_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, rare, harrisons_view_member, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_hereditary_disease, ordo_group_of_disorders, harrisons_view_integumentary_system_disorder

exactMatch

http://www.orpha.net/ORDO/Orphanet_79357

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1941547119

http://identifiers.org/medgen/590657

http://identifiers.org/snomedct/239066003

http://linkedlifedata.com/resource/umls/id/C0406757

id

MONDO:0019272