Lymphoblastic leukemia, acute, with lymphomatous features

Preferred Label : Lymphoblastic leukemia, acute, with lymphomatous features;

Symbol : LALL;

CISMeF acronym : LALL;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Lymphomatous all;

Inheritance : Acquired specific neoplasm by autosomal recessive mechanism through somatic cell mutation;

Prefixed ID : 247640;

Details

Origin ID

247640;

UMLS CUI

C1855472;

Automatic exact mappings (from CISMeF team)
- Lalling (finding) [SNOMED CT concept]
- Phonological disorder [ICD-10 Sub-category]
- Precursor T-cell acute lymphoblastic leukemia [ORDO Disease]
- lalling [SNOMED Notion]
Currated CISMeF NLP mapping
- lymphoblastic leukemia, acute, with lymphomatous features [MeSH concept]
- lymphoblastic leukemia, acute, with lymphomatous features [MeSH Supplementary Concept]
DO Cross reference
- acute lymphoblastic leukemia [DO Concept]
HPO term(s)
- Acute lymphoblastic leukemia [HPO term]
- Autosomal recessive inheritance [HPO term]
- Lymphoma [HPO term]
- T-cell acute lymphoblastic leukemias [HPO term]
ORDO concept(s)
- Acute lymphoblastic leukemia [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- lymphoblastic leukemia, acute, with lymphomatous features [MeSH Supplementary Concept]
- lymphoblastic leukemia, acute, with lymphomatous features [MeSH concept]

Keyword's position in hierarchy(ies) :

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