ehlers-danlos syndrome, nos - CISMeF

CISMeF

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Ehlers-danlos syndrome, nosSNOMED Notion

Preferred Label : ehlers-danlos syndrome, nos;

Details

Origin ID

D6-90100;

UMLS CUI

C0013720;

Automatic exact mappings (from CISMeF team)
- Emergency Department (DEEDS) variables [LOINC Class]
- Emergency department [LOINC System]
- musculoskeletal disease other [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Ehlers Danlos syndrome [PASCAL descriptor]
- Ehlers Danlos syndrome [Disease (Nov.)]
- Ehlers-Danlos Syndrome [NCIt concept]
- Ehlers-Danlos syndrome [ICD-10 Sub-category]
- Ehlers-Danlos syndrome [DO Concept]
- Ehlers-Danlos syndrome [ICD-11 Subcategory]
- Ehlers-Danlos syndrome [ICD-9 code]
- Ehlers-Danlos syndrome [MeSH concept]
- Ehlers-Danlos syndrome [ICD-10 Sub-category (who)]
- Ehlers-Danlos syndrome [MedDRA Preferred Term]
- Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-Danlos syndrome (disorder) [SNOMED CT concept]
- Ehlers-danlos syndrome [OMIM phenotypic series]
- ehlers-danlos syndrome [MeSH Descriptor]
- ehlers-danlos syndrome [MedlinePlus Topic]
ICD-10 exact mapping(s)
- Ehlers-Danlos syndrome [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Arthrochalasia Ehlers-Danlos syndrome [ORDO Disease]
- B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome [ORDO Disease]
- Classical Ehlers-Danlos syndrome [ORDO Disease]
- Dermatosparaxis Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-Danlos syndrome with periventricular heterotopia [ORDO Disease]
- Ehlers-Danlos syndrome, fibronectinemic type [ORDO Disease]
- Hypermobile Ehlers-Danlos syndrome [ORDO Disease]
- Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency [ORDO Disease]
- Periodontal Ehlers-Danlos syndrome [ORDO Disease]
- SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Dermis elastic tissue disorder [ORDO Disease]
- Lens position anomaly [ORDO Disease]
- Rare developmental defect with connective tissue involvement [ORDO Disease]
- Rare developmental defect with skin/mucosae involvement [ORDO Disease]
- Syndromic epicanthus [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cutis hyperplastica [MedDRA LLT]
- Ehlers Danlos syndrome [Disease (Nov.)]
- Ehlers Danlos syndrome [PASCAL descriptor]
- Ehlers-Danlos Syndrome [NCIt concept]
- Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-Danlos syndrome [ICD-10 Sub-category]
- Ehlers-Danlos syndrome [MeSH concept]
- Ehlers-Danlos syndrome [DO Concept]
- Ehlers-Danlos syndrome [ICD-9 code]
- Ehlers-Danlos syndrome [ICD-11 Subcategory]
- Ehlers-Danlos syndrome [ICD-10 Sub-category (who)]
- Ehlers-Danlos syndrome [MedDRA Preferred Term]
- Ehlers-Danlos syndrome (disorder) [SNOMED CT concept]
- ehlers-danlos syndrome [MedlinePlus Topic]
- ehlers-danlos syndrome [MeSH Descriptor]
Validated automatic mappings to BTNT
- Ehlers-Danlos syndrome of undetermined or unspecified type [ICD-11 More detail]

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06/09/2025

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