abnormalities - CISMeF

Preferred Label : abnormalities;

MeSH synonym : agenesis; anomalies; aplasia; atresia; birth defects; congenital defects; defects; deformities; hypoplasia; malformations; teratology;

Details

Origin ID

Q000002;

UMLS CUI

C0000769;

Automatic exact mappings (from CISMeF team)
- AB hearing assessment list (physical object) [SNOMED CT concept]
- Abnormal [NCIt concept]
- Abnormal (qualifier value) [SNOMED CT concept]
- Abnormal Reference Range [NCIt concept]
- Acromesomelic dysplasia group (disorder) [SNOMED CT concept]
- Acromicric dysplasia (disorder) [SNOMED CT concept]
- Agenesis [PASCAL descriptor]
- Agenesis [NCIt concept]
- Anismus (disorder) [SNOMED CT concept]
- Anomaly congenital [MedDRA LLT]
- Aplasia [PASCAL descriptor]
- Aplasia [MedDRA Preferred Term]
- Aplasia (morphologic abnormality) [SNOMED CT concept]
- Aplasia NOS [MedDRA LLT]
- Aplasia, other [ACR pathology]
- Atresia [PASCAL descriptor]
- Atresia [NCIt concept]
- Atresia [ACR pathology]
- Atresia [ACR pathology]
- Atresia, other [ACR pathology]
- Birth defects [LOINC method]
- Birth defects [MedDRA LLT]
- Bladder neck dyssynergia (disorder) [SNOMED CT concept]
- CONGENITAL ANOMALY NOS [WHO-ART Preferred Term]
- Cementoma (morphologic abnormality) [SNOMED CT concept]
- Chondroectodermal dysplasia (disorder) [SNOMED CT concept]
- Congenital Abnormality [NCIt concept]
- Congenital abnormal roundness (morphologic abnormality) [SNOMED CT concept]
- Congenital abnormality NOS [MedDRA LLT]
- Congenital absence (morphologic abnormality) [SNOMED CT concept]
- Congenital anomaly [MedDRA Preferred Term]
- Congenital anomaly (morphologic abnormality) [Inactive SNOMED CT concept]
- Congenital anomaly NOS [MedDRA LLT]
- Congenital anomaly of integument (disorder) [SNOMED CT concept]
- Congenital anomaly of joint (disorder) [SNOMED CT concept]
- Congenital anomaly of lens (disorder) [SNOMED CT concept]
- Congenital anomaly of scapula (disorder) [SNOMED CT concept]
- Congenital anomaly, unspecified [ICD-9 code]
- Congenital atresia (morphologic abnormality) [SNOMED CT concept]
- Congenital atrophy of optic nerve (disorder) [SNOMED CT concept]
- Congenital deficiency (morphologic abnormality) [Inactive SNOMED CT concept]
- Congenital hip dysplasia (disorder) [SNOMED CT concept]
- Congenital malformation (disorder) [SNOMED CT concept]
- Congenital malformation (morphologic abnormality) [Inactive SNOMED CT concept]
- Congenital malformation of genital organs (disorder) [SNOMED CT concept]
- Congenital malformation, unspecified [ICD-10 Sub-category (who)]
- Congenital or Acquired Anatomic Abnormality [NCIt concept]
- Defect [NCIt concept]
- Defect (morphologic abnormality) [SNOMED CT concept]
- Deformation [PASCAL descriptor]
- Deformity [MedDRA Preferred Term]
- Deformity (finding) [SNOMED CT concept]
- Deformity (morphologic abnormality) [SNOMED CT concept]
- Developmental anomaly (morphologic abnormality) [SNOMED CT concept]
- Diffuse glomerulosclerosis (morphologic abnormality) [SNOMED CT concept]
- Dysmorphism (disorder) [SNOMED CT concept]
- Familial caudal dysgenesis (disorder) [SNOMED CT concept]
- Foetal malformation [MedDRA Preferred Term]
- HYPOPLASIA [ACR pathology]
- Hypoplasia [PASCAL descriptor]
- Hypoplasia [NCIt concept]
- Hypoplasia [ACR pathology]
- Hypoplasia [ACR pathology]
- Hypoplasia [ACR pathology]
- Hypoplasia [ACR pathology]
- Hypoplasia (morphologic abnormality) [SNOMED CT concept]
- Hypoplasia, other [ACR pathology]
- Idiopathic detrusor overactivity (disorder) [SNOMED CT concept]
- Jarcho-Levin syndrome (disorder) [SNOMED CT concept]
- Malformation [PASCAL descriptor]
- Malformations [PASCAL theme]
- Malformations [PASCAL theme]
- Malformations [PASCAL theme]
- Malformations [PASCAL theme]
- Monostotic fibrous dysplasia (disorder) [SNOMED CT concept]
- Oculoskeletal dysplasia (disorder) [SNOMED CT concept]
- Other congenital anomaly NOS [MedDRA LLT]
- Patellar clunk syndrome (disorder) [SNOMED CT concept]
- Pelvic lymphangiography, bilateral (procedure) [SNOMED CT concept]
- Percent of Abnormal Cells [NCIt concept]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- Rare teratologic disease [ORDO Disease]
- TP53 Gene Mutation [NCIt concept]
- Teratology [NCIt concept]
- Transitional cell dysplasia (morphologic abnormality) [SNOMED CT concept]
- abnormal [Radlex concept]
- agenesis [Radlex concept]
- aplasia [Radlex concept]
- aplasia, nos [SNOMED Notion]
- atresia [Radlex concept]
- birth defects [MedlinePlus Topic]
- congenital deficiency, nos [SNOMED Notion]
- defect, nos [SNOMED Notion]
- deformity [Radlex concept]
- deformity [VCM modifier]
- deformity, nos [SNOMED Notion]
- developmental anomaly [Artificial nutrition thesaurus concept]
- developmental anomaly, nos [SNOMED Notion]
- distorted [Radlex concept]
- dysgenesis [Radlex concept]
- hypoplasia, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- Abnormality [NCIt concept]
False automatic mappings
- Molecular Genetic Variation [NCIt concept]
- Thyroid hormone plasma membrane transport defect [OMIM Phenotype]
- aplasia [Disease (Nov.)]
Mapping VCM hiérarchique
- deformity [VCM modifier]
See also
- congenital abnormalities [MeSH Descriptor]
See also inter- (CISMeF)
- Agenesis (morphologic abnormality) [SNOMED CT concept]
- deformity [Disease (Nov.)]
- hypoplasia [Disease (Nov.)]
Semantic type(s)
- Functional Concept [UMLS semantic type]
Validated automatic mappings to BTNT
- Deformity (finding) [SNOMED CT concept]
- agenesis [Disease (Nov.)]
- atresia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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