porokeratosis - CISMeF

Preferred Label : porokeratosis;

MeSH definition : A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis.;

MeSH hyponym : porokeratosis, linear; porokeratosis, punctate; porokeratosis, palmoplantar; porokeratosis, mibelli; porokeratosis, disseminated superficial actinic; Disseminated Superficial Actinic Porokeratosis; Palmoplantar Porokeratosis; Keratoderma Palmoplantar, Punctate Type 2; Porokeratosis Plantaris, Palmaris, Et Disseminata; Porokeratosis Plantaris Palmaris et Disseminata; Porokeratosis, Palmar, Plantar, And Disseminated 1; Porokeratosis Palmaris et Plantaris Disseminata; Type 2 Punctate PPK; Linear Porokeratosis; Mibelli Porokeratosis; Porokeratosis of Mibelli; Punctate Porokeratosis;

Related MeSH term : Porokeratosis, disseminated superficial actinic 2; Porokeratosis, Disseminated Superficial Actinic, 2;

MeSH annotation : do not confuse with PARAKERATOSIS;

Wikipedia link : https://en.wikipedia.org/wiki/Porokeratosis;

Details

Origin ID

D017499;

UMLS CUI

C0162839;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Disseminated superficial actinic porokeratosis [ICD-11 More detail]
- Disseminated superficial actinic porokeratosis [MedDRA Preferred Term]
- Disseminated superficial actinic porokeratosis [ORDO Disease]
- Disseminated superficial actinic porokeratosis (disorder) [SNOMED CT concept]
- Linear porokeratosis [PASCAL descriptor]
- Linear porokeratosis [ICD-11 More detail]
- Linear porokeratosis (disorder) [SNOMED CT concept]
- Localised porokeratosis [ICD-11 More detail]
- Mibelli porokeratosis [PASCAL descriptor]
- Other specified congenital malformations of skin [ICD-10 Sub-category (who)]
- Palmoplantar porokeratosis [PASCAL descriptor]
- Porokeratoses [ICD-11 Category]
- Porokeratosis [OMIM phenotypic series]
- Porokeratosis 1, multiple types [OMIM Phenotype]
- Porokeratosis 4, disseminated superficial actinic type [OMIM Phenotype]
- Porokeratosis of Mantoux (disorder) [Inactive SNOMED CT concept]
- Porokeratosis of Mibelli [ORDO Disease]
- Porokeratosis of Mibelli (disorder) [SNOMED CT concept]
- Porokeratosis palmaris, plantaris et disseminata [PASCAL descriptor]
- Porokeratosis plantaris palmaris et disseminata [ORDO Disease]
- Porokeratosis plantaris palmaris et disseminata (disorder) [SNOMED CT concept]
- Punctate palmoplantar keratoderma type 2 [ORDO Disease]
- Punctate palmoplantar keratoderma type 2 (disorder) [SNOMED CT concept]
- Punctate palmoplantar keratoderma, type 2 [ICD-11 More detail]
- disseminated superficial actinic porokeratosis [SNOMED Notion]
- porokeratosis of mibelli [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital pigmentary anomalies of skin [ICD-9 code]
- Porokeratosis [PASCAL descriptor]
- Porokeratosis [HPO term]
- Porokeratosis [MedDRA Preferred Term]
- Porokeratosis [NCIt concept]
- Porokeratosis [ORDO Disease]
- Porokeratosis (disorder) [SNOMED CT concept]
- porokeratosis [DO Concept]
- porokeratosis [Disease (Nov.)]
DO Cross reference
- porokeratosis [DO Concept]
HPO term
- Porokeratosis [HPO term]
Has phenotype(s) (HPO)
- Histological abnormality of the skin [HPO term]
Manual NTBT mappings (CISMeF)
- Epidermal disease [ORDO Disease]
- Genetic porokeratosis [ORDO Disease]
- Hereditary palmoplantar keratoderma [ORDO Disease]
Ne pas confondre avec
- keratoderma, palmoplantar [MeSH Descriptor]
- parakeratosis [MeSH Descriptor]
ORDO relation(s)
- Porokeratosis [ORDO Disease]
Record concept(s)
- Porokeratosis, disseminated superficial actinic 2 [MeSH concept]
- porokeratosis [MeSH concept]
- porokeratosis, disseminated superficial actinic [MeSH concept]
- porokeratosis, linear [MeSH concept]
- porokeratosis, mibelli [MeSH concept]
- porokeratosis, palmoplantar [MeSH concept]
- porokeratosis, punctate [MeSH concept]
Related MeSH Supplementary Concept(s)
- congenital facial linear porokeratosis [MeSH Supplementary Concept]
- craniosynostosis, anal anomalies, and porokeratosis [MeSH Supplementary Concept]
- porokeratosis punctata palmaris et plantaris [MeSH Supplementary Concept]
- porokeratosis, disseminated superficial actinic 1 [MeSH Supplementary Concept]
- porokeratosis, disseminated superficial actinic, 3 [MeSH Supplementary Concept]
- porokeratosis, disseminated superficial actinic, 4 [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Porokeratosis [ORDO Disease]
- Porokeratosis [MedDRA Preferred Term]
- Porokeratosis [HPO term]
- Porokeratosis [NCIt concept]
- Porokeratosis (disorder) [SNOMED CT concept]
Validated automatic mappings to BTNT
- Linear porokeratosis (disorder) [SNOMED CT concept]
- Porokeratosis 2, palmar, plantar, and disseminated type [OMIM Phenotype]
- Porokeratosis palmaris, plantaris et disseminata [PASCAL descriptor]
- disseminated superficial actinic porokeratosis [Disease (Nov.)]
- linear porokeratosis [Disease (Nov.)]
- porokeratosis of Mantoux [Disease (Nov.)]
- porokeratosis of Mibelli [Disease (Nov.)]
- punctate porokeratosis [Disease (Nov.)]

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