Letterer-siwe disease

Preferred Label : Letterer-siwe disease;

CISMeF acronym : LESD;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : L-s disease; Histiocytosis X, acute disseminated; LESD;

Inheritance : Autosomal recessive;

Prefixed ID : %246400;

Details

Origin ID

246400;

UMLS CUI

C0023381;

Automatic exact mappings (from CISMeF team)
- Familial Letterer-Siwe disease [MeSH concept]
- Langerhans cell histiocytosis, disseminated (morphologic abnormality) [SNOMED CT concept]
- Langerhans-cell histiocytosis [DO Concept]
- Letterer Siwe disease [PASCAL descriptor]
- Letterer-Siwe disease [ICD-11 Extension code]
- Letterer-Siwe disease [ICD-11 Extension code]
- Letterer-Siwe disease [ICD-9 code]
- Letterer-Siwe disease [ACR pathology]
- Letterer-Siwe disease [ACR pathology]
- Letterer-Siwe disease [ACR pathology]
- familial Letterer-Siwe disease [MeSH Supplementary Concept]
- histiocytosis, Langerhans-Cell [MeSH Descriptor]
- histiocytosis, Langerhans-Cell [MeSH concept]
Currated CISMeF NLP mapping
- Letterer-Siwe Disease [NCIt concept]
- Letterer-Siwe disease [ICD-10 Sub-category (who)]
- Letterer-Siwe disease [Radlex concept]
- Letterer-Siwe disease [ORDO Disease]
- Letterer-Siwe disease [MedDRA LLT]
- Letterer-Siwe's disease [ICD-9 code]
- Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis [ICD-10 Sub-category]
DO Cross reference
- Langerhans-cell histiocytosis [DO Concept]
HPO term(s)
- Abdominal distention [HPO term]
- Abnormality of the skeletal system [HPO term]
- Anemia [HPO term]
- Autosomal recessive inheritance [HPO term]
- Dyspnea [HPO term]
- Encephalopathy [HPO term]
- Fever [HPO term]
- Hepatosplenomegaly [HPO term]
- Irritability [HPO term]
- Jaundice [HPO term]
- Neutropenia [HPO term]
- Pallor [HPO term]
- Pulmonary infiltrates [HPO term]
- Seborrheic dermatitis [HPO term]
- Stomatitis [HPO term]
- Thrombocytopenia [HPO term]
ORDO concept(s)
- Letterer-Siwe disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Letterer-Siwe disease [MeSH concept]
- Langerhans cell histiocytosis, disseminated [ICD-O code]
- Langerhans cell histiocytosis, disseminated (disorder) [SNOMED CT concept]
- Langerhans cell histiocytosis, disseminated (morphologic abnormality) [SNOMED CT concept]
- Letterer-Siwe Disease [NCIt concept]
- Letterer-Siwe disease [ICD-10 Sub-category (who)]
- Letterer-Siwe disease [ORDO Disease]
- Letterer-Siwe disease [MedDRA LLT]
- Letterer-Siwe disease [ICD-9 code]
- Letterer-Siwe disease [Radlex concept]
- familial Letterer-Siwe disease [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- langerhans cell histiocytosis [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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