Congenital cutaneous mastocytosis

Preferred Label : Congenital cutaneous mastocytosis;

Inclusion CIM-10 : Congenital diffuse cutaneous mastocytosis; Congenital urticaria pigmentosa; Congenital maculopapular cutaneous mastocytosis;

ICD-10 exclusion note : malignant mastocytosis (C96.2-); cutaneous mastocytosis NOS (D47.01); diffuse cutaneous mastocytosis (with onset after newborn period) (D47.01); urticaria pigmentosa (non-congenital) (with onset after newborn period) (D47.01); systemic mastocytosis (D47.02);

Diag associé à un acte (%) : 78.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q822;

UMLS CUI

C5779617;

CISMeF manual mappings
- Mast cell disorder (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Mast Cell Neoplasm [NCIt concept]
- Mastocytosis [NCIt concept]
- Mastocytosis [HPO term]
- Mastocytosis [ORDO Disease]
- Mastocytosis [MedDRA Preferred Term]
- Mastocytosis [HRDO Sign]
- Mastocytosis [PASCAL descriptor]
- Mastocytosis [ICD-11 Category]
- mastocytosis [MeSH concept]
- mastocytosis [MeSH Descriptor]
- mastocytosis [Disease (Nov.)]
Excluded by
- Malignant mast cell neoplasm [ICD-10 Sub-category]
- Mast cell neoplasms of uncertain behavior [ICD-10 Sub-category]
- Urticaria [ICD-10 category]
ICD-10 exclusion(s)
- Malignant mast cell neoplasm [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Indolent systemic mastocytosis [ORDO Disease]
- Systemic mastocytosis with associated hematologic neoplasm [ORDO Disease]
Orphanet concepts
- Bloom syndrome [ORDO Disease]
- Bullous diffuse cutaneous mastocytosis [ORDO Disease]
- Cutaneous mastocytoma [ORDO Disease]
- Cutaneous mastocytosis [ORDO Disease]
- Diffuse cutaneous mastocytosis [ORDO Disease]
- Hennekam-Beemer syndrome [ORDO Disease]
- Maculopapular cutaneous mastocytosis [ORDO Disease]
- Mastocytosis [ORDO Disease]
- Nodular urticaria pigmentosa [ORDO Disease]
- Plaque-form urticaria pigmentosa [ORDO Disease]
- Pseudoxanthomatous diffuse cutaneous mastocytosis [ORDO Disease]
- Pure hair and nail ectodermal dysplasia [ORDO Disease]
- Telangiectasia macularis eruptiva perstans [ORDO Disease]
- Typical urticaria pigmentosa [ORDO Disease]
See also inter- (CISMeF)
- Extracutaneous mastocytoma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Mast cell activation syndrome [MedDRA Preferred Term]
- Mast cell disorder (disorder) [SNOMED CT concept]
- Mast cell hyperplasia (morphologic abnormality) [SNOMED CT concept]
- Mastocytosis [MedDRA Preferred Term]
- Mastocytosis [HPO term]
- Mastocytosis [NCIt concept]
- Mastocytosis [ORDO Disease]
- Mastocytosis, cutaneous [OMIM Phenotype]
- mast cell activation syndrome [Disease (Nov.)]
- mastocytosis [MeSH Descriptor]
- mastocytosis [MeSH concept]
- mastocytosis [DO Concept]
- mastocytosis [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients