lymphangiomyomatosis

Preferred Label : lymphangiomyomatosis;

Origin ID

M-91741;

UMLS CUI

C0751674;

Automatic exact mappings (from CISMeF team)
- Lymphangiomyomatosis [ICD-11 Extension code]
- Lymphangiomyomatosis [ICD-O code]
Currated CISMeF NLP mapping
- Lymphangioleiomyomatosis [MedDRA Preferred Term]
- Lymphangioleiomyomatosis [NCIt concept]
- Lymphangioleiomyomatosis [OMIM Phenotype]
- Lymphangioleiomyomatosis [ORDO Disease]
- Lymphangiomyomatosis [MedDRA LLT]
- Lymphangiomyomatosis (morphologic abnormality) [SNOMED CT concept]
- lymphangioleiomyomatosis [Radlex concept]
- lymphangioleiomyomatosis [DO Concept]
- lymphangioleiomyomatosis [MeSH Descriptor]
- lymphangioleiomyomatosis [MeSH concept]
Manual NTBT mappings (CISMeF)
- Rare genetic respiratory disease [ORDO Disease]
- Rare pulmonary hypertension [ORDO Disease]
SNOMED CT concept
- Lymphangiomyomatosis (morphologic abnormality) [SNOMED CT concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Lymphangioleiomyomatosis [MedDRA Preferred Term]
- Lymphangioleiomyomatosis [ICD-9 code]
- Lymphangioleiomyomatosis [ORDO Disease]
- Lymphangioleiomyomatosis [OMIM Phenotype]
- Lymphangioleiomyomatosis [ICD-11 Category]
- Lymphangioleiomyomatosis [NCIt concept]
- Lymphangiomyomatosis [MedDRA LLT]
- Lymphangiomyomatosis (morphologic abnormality) [SNOMED CT concept]
- lymphangioleiomyomatosis [Radlex concept]
- lymphangioleiomyomatosis [MeSH concept]
- lymphangioleiomyomatosis [Disease (Nov.)]
- lymphangioleiomyomatosis [MeSH Descriptor]