Mucinosis of the skin

Preferred Label : Mucinosis of the skin;

Inclusion CIM-10 : Focal mucinosis; Lichen myxedematosus; Reticular erythematous mucinosis;

ICD-10 exclusion note : focal oral mucinosis (K13.79); myxedema (E03.9);

Diag associé à un acte (%) : 87.5;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Date de mise à jour : 01/01/2014;

Details

Origin ID

L985;

UMLS CUI

C0406655;

Automatic exact mappings (from CISMeF team)
- Cutaneous mucinosis [ICD-11 Subcategory]
- Diffuse cutaneous mucinosis (disorder) [SNOMED CT concept]
- Lichen myxedematosus [ORDO Disease]
- Lichen myxedematosus [MedDRA LLT]
- Lichen myxedematosus (disorder) [SNOMED CT concept]
- Mucinosis affecting skin (disorder) [SNOMED CT concept]
- Reticular erythematous mucinosis [ICD-11 Sub-sub category]
- Reticular erythematous mucinosis [MedDRA Preferred Term]
- Reticular erythematous mucinosis (disorder) [SNOMED CT concept]
- scleromyxedema [MeSH Descriptor]
ICD-10 exclusion(s)
- Hypothyroidism, unspecified [ICD-10 Sub-category]
- Other and unspecified lesions of oral mucosa [ICD-10 Sub-category]
Orphanet concepts
- Acral persistent papular mucinosis [ORDO Disease]
- Atypical lichen myxedematosus [ORDO Disease]
- Discrete papular lichen myxedematosus [ORDO Disease]
- Lichen myxedematosus [ORDO Disease]
- Localized lichen myxedematosus [ORDO Disease]
- Localized lichen myxedematosus with mixed features of different subtypes [ORDO Disease]
- Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms [ORDO Disease]
- Nodular lichen myxedematosus [ORDO Disease]
- Papular mucinosis of infancy [ORDO Disease]
- Scleromyxedema [ORDO Disease]
- Scleromyxedema without monoclonal gammopathy [ORDO Disease]
- Self-healing papular mucinosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cutaneous mucinosis [ICD-11 Subcategory]
- Diffuse cutaneous mucinosis (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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