lymphedema - CISMeF

Preferred Label : lymphedema;

MeSH definition : Edema due to obstruction of lymph vessels or disorders of the lymph nodes.;

MeSH synonym : lymphedemas;

CISMeF synonym : disease, milroy's; disease, milroy;

MeSH hyponym : milroy disease; Early Onset Lymphedema; Early Onset Lymphedemas; Lymphedemas, Early Onset; Hereditary Lymphedema; Hereditary Lymphedemas; Lymphedema, Hereditary; Lymphedemas, Hereditary; Hereditary Lymphedema 1; Hereditary Lymphedema 1s; Lymphedema, Early-Onset; Early-Onset Lymphedema; Early-Onset Lymphedemas; Lymphedema, Early Onset; Lymphedemas, Early-Onset; Hereditary Lymphedema Type I; Milroy's Disease; Milroys Disease; Nonne-Milroy Disease; Nonne Milroy Disease; Nonne-Milroy Lymphedema; Lymphedema, Nonne-Milroy; Nonne Milroy Lymphedema; Nonne-Milroy-Meige Disease; Nonne Milroy Meige Disease; Primary Congenital Lymphedema; Congenital Lymphedema, Primary; Congenital Lymphedemas, Primary; Lymphedema, Primary Congenital; Lymphedemas, Primary Congenital; Primary Congenital Lymphedemas; Congenital Familial Lymphedema; Congenital Hereditary Lymphedema; Congenital Hereditary Lymphedemas; Hereditary Lymphedema, Congenital; Hereditary Lymphedemas, Congenital; Lymphedema, Congenital Hereditary; Lymphedemas, Congenital Hereditary; Lymphedema, Hereditary, Ia;

MeSH annotation : entry term MILROY'S DISEASE goes under LYMPHEDEMA/ congen;

Wikipedia link : https://en.wikipedia.org/wiki/Lymphedema;

Details

Origin ID

D008209;

UMLS CUI

C0024236;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Congenital primary lymphoedema [ICD-11 More detail]
- Dermatopathic lymphadenopathy [ICD-11 More detail]
- Facial lymphedema (disorder) [SNOMED CT concept]
- Hereditary lymphedema [ICD-10 Sub-category]
- Hereditary lymphedema (disorder) [SNOMED CT concept]
- Hereditary lymphedema type I (disorder) [SNOMED CT concept]
- Hereditary lymphoedema [ICD-10 Sub-category (who)]
- Lymphedema, CTCAE [NCIt concept]
- Milroy disease [ACR pathology]
- Milroy disease [ORDO Disease]
- Milroy's disease [MedDRA LLT]
- Trophoedema [MedDRA LLT]
- cardiovascular disease other [ICPC-2 Rubric]
- fms related receptor tyrosine kinase 4 [HGNC gene]
- hereditary edema of legs [SNOMED Notion]
- hereditary lymphedema [DO Concept]
- hereditary lymphedema I [DO Concept]
- hereditary lymphedema IA [DO Concept]
Currated CISMeF NLP mapping
- LYMPHEDEMA [ACR pathology]
- LYMPHOEDEMA [WHO-ART Preferred Term]
- Lymphatic Oedema [ICNP subject]
- Lymphatic Oedema [ICNP diagnostic]
- Lymphatic edema (morphologic abnormality) [SNOMED CT concept]
- Lymphedema [PASCAL descriptor]
- Lymphedema [NCIt concept]
- Lymphedema [ACR pathology]
- Lymphedema [HPO term]
- Lymphedema [ORDO Disease]
- Lymphedema [MedDRA LLT]
- Lymphedema [HRDO Sign]
- Lymphedema (disorder) [SNOMED CT concept]
- Lymphoedema [ICD-11 Category]
- Lymphoedema [MedDRA Preferred Term]
- Lymphoedema NOS [MedDRA LLT]
- Lymphoedemas [MedDRA High Level Term]
- lymphatic edema [SNOMED Notion]
- lymphedema [DO Concept]
- lymphedema [Disease (Nov.)]
- lymphedema [Radlex concept]
- lymphedema [MedlinePlus Topic]
- lymphedema [LOINC part]
DO Cross reference
- hereditary lymphedema I [DO Concept]
- lymphedema [DO Concept]
HPO term
- Lymphedema [HPO term]
Manual BTNT mappings - CISMeF
- Lipedema [ORDO Disease]
- Primary lymphedema [ORDO Disease]
- Syndromic lymphedema [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare genetic skin disease [ORDO Disease]
- Rare skin disease [ORDO Disease]
MedlinePlus topic(s)
- lymphedema [MedlinePlus Topic]
ORDO relation(s)
- Lymphedema [ORDO Disease]
Record concept(s)
- lymphedema [MeSH concept]
- milroy disease [MeSH concept]
Related MeSH Supplementary Concept(s)
- Aagenaes syndrome [MeSH Supplementary Concept]
- Hypotrichosis-Lymphedema-Telangiectasia syndrome [MeSH Supplementary Concept]
- Lymphedema-Distichiasis syndrome with renal disease and diabetes mellitus [MeSH Supplementary Concept]
- dahlberg borer newcomer syndrome [MeSH Supplementary Concept]
- ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema [MeSH Supplementary Concept]
- german syndrome [MeSH Supplementary Concept]
- hennekam lymphangiectasia lymphedema syndrome [MeSH Supplementary Concept]
- irons bhan syndrome [MeSH Supplementary Concept]
- lymphedema and cerebral arteriovenous anomaly [MeSH Supplementary Concept]
- lymphedema distichiasis syndrome [MeSH Supplementary Concept]
- lymphedema, cardiac septal defects, and characteristic facies [MeSH Supplementary Concept]
- lymphedema, congenital recessive [MeSH Supplementary Concept]
- lymphedema, hereditary, IB [MeSH Supplementary Concept]
- lymphedema, hereditary, II [MeSH Supplementary Concept]
- lymphedema, microcephaly and chorioretinopathy syndrome [MeSH Supplementary Concept]
- waldmann disease [MeSH Supplementary Concept]
See also
- Lipedema [MeSH Descriptor]
- edema [MeSH Descriptor]
- yellow nail syndrome [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chronic lymphovenous insufficiency [MedDRA LLT]
- LYMPHEDEMA [ACR pathology]
- LYMPHOEDEMA [WHO-ART Preferred Term]
- Lymphatic Oedema [ICNP diagnostic]
- Lymphatic edema (morphologic abnormality) [SNOMED CT concept]
- Lymphedema [ORDO Disease]
- Lymphedema [HPO term]
- Lymphedema [ACR pathology]
- Lymphedema [HRDO Sign]
- Lymphedema [PASCAL descriptor]
- Lymphedema [NCIt concept]
- Lymphedema [MedDRA LLT]
- Lymphedema (disorder) [SNOMED CT concept]
- Lymphoedema [MedDRA Preferred Term]
- Lymphoedema [ICD-11 Category]
- Lymphoedema NOS [MedDRA LLT]
- Lymphoedemas [MedDRA High Level Term]
- lymphatic edema [SNOMED Notion]
- lymphedema [DO Concept]
- lymphedema [Disease (Nov.)]
- lymphedema [LOINC part]
- lymphedema [MedlinePlus Topic]
Validated automatic mappings to BTNT
- Congenital primary lymphedema without systemic or visceral involvement [ORDO Disease]
- Lymphatic malformation 1 [OMIM Phenotype]
- Lymphatic malformation 5 [OMIM Phenotype]
- Trophedema [MedDRA LLT]

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