Description
skin disease: Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs.
Data source
| FinnGen phenocode |
L12_OTHERSKINSUBCUTIS |
| Include |
L12_VITILIGO, L12_OTHPIGMENTATION, L12_SEBORRKERAT, L12_ACANTHNIGRICANS, L12_CORNSANDCALLOS, L12_EPIDERMALTHICKOTH, L12_ACQICTHY, L12_ACQKERAT, L12_KERATPUNCTATA, L12_XEROSCUT, L12_EPIDERMTHICKNAS, L12_KERATODERMAINOTH, L12_TRANSEPIDERMELIMINATION, L12_PYODERMAGANGRENOSUM, L12_DECUBITANSULCERANDPRESSURE, L12_ATROPHICSKIN, L12_LICHENSCLERATROPH, L12_ANETODERMA, L12_ATROPODERMAPASINI, L12_ACRODERMATITIS, L12_SCARCONDITIONS, L12_STRIAEATROPHICAE, L12_ATROPHICSKINNAS, L12_HYPERTROPHICSKIN, L12_GRANULOMATOUSSKIN, L12_LUPUS, L12_LOCALDCONNECTISSUEOTH, L12_VASCULITISSKIN, L12_ULCERLOWLIMB, L12_OTHERDISSKINANDSUBCUTIS, L12_SKININOTH |
| Level in the ICD-hierarchy |
2 |
| First defined in version |
DF2 |
Ontology