dysgenesis - CISMeF

Preferred Label : dysgenesis;

Definition : defective or abnormal development of an organ;

UMLS CUI (RADLEX) : C0000768;

Details

Origin ID

RID3741;

UMLS CUI

C0000768;

Associated condition of
- empty mediastinum sign [Radlex concept]
Automatic exact mappings (from CISMeF team)
- Acromesomelic dysplasia group (disorder) [SNOMED CT concept]
- Acromicric dysplasia (disorder) [SNOMED CT concept]
- Anismus (disorder) [SNOMED CT concept]
- Bladder neck dyssynergia (disorder) [SNOMED CT concept]
- Cementoma (morphologic abnormality) [SNOMED CT concept]
- Chondroectodermal dysplasia (disorder) [SNOMED CT concept]
- Congenital abnormal roundness (morphologic abnormality) [SNOMED CT concept]
- 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 atrophy of optic nerve (disorder) [SNOMED CT concept]
- Congenital hip dysplasia (disorder) [SNOMED CT concept]
- Congenital malformation of genital organs (disorder) [SNOMED CT concept]
- Congenital malformation, unspecified [ICD-10 Sub-category (who)]
- Diffuse glomerulosclerosis (morphologic abnormality) [SNOMED CT concept]
- Dysgenesis [PASCAL descriptor]
- Familial caudal dysgenesis (disorder) [SNOMED CT concept]
- Idiopathic detrusor overactivity (disorder) [SNOMED CT concept]
- Jarcho-Levin syndrome (disorder) [SNOMED CT concept]
- 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]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- Transitional cell dysplasia (morphologic abnormality) [SNOMED CT concept]
- abnormalities [MeSH Qualifier]
Currated CISMeF NLP mapping
- Anomaly congenital [MedDRA LLT]
- CONGENITAL ANOMALIES [ICD-9 code]
- CONGENITAL ANOMALY NOS [WHO-ART Preferred Term]
- Congenital abnormality NOS [MedDRA LLT]
- Congenital anomaly [MedDRA Preferred Term]
- Congenital anomaly (morphologic abnormality) [Inactive SNOMED CT concept]
- Congenital anomaly NOS [MedDRA LLT]
- Congenital anomaly, unspecified [ICD-9 code]
- Congenital deformity (disorder) [SNOMED CT concept]
- Congenital malformation (disorder) [SNOMED CT concept]
- Congenital malformation (morphologic abnormality) [Inactive SNOMED CT concept]
- Developmental anomaly (morphologic abnormality) [SNOMED CT concept]
- congenital abnormalities [MeSH Descriptor]
- developmental anomaly [Artificial nutrition thesaurus concept]
- developmental anomaly, nos [SNOMED Notion]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Anomaly congenital [MedDRA LLT]
- Birth defects [MedDRA LLT]
- CONGENITAL ANOMALIES [ICD-9 code]
- CONGENITAL ANOMALY NOS [WHO-ART Preferred Term]
- Congenital Abnormality [NCIt concept]
- Congenital abnormality NOS [MedDRA LLT]
- Congenital anomaly [MedDRA Preferred Term]
- Congenital anomaly (disorder) [Inactive SNOMED CT concept]
- Congenital anomaly (morphologic abnormality) [Inactive SNOMED CT concept]
- Congenital anomaly NOS [MedDRA LLT]
- Congenital anomaly, unspecified [ICD-9 code]
- Congenital deformity (disorder) [SNOMED CT concept]
- Congenital deformity (morphologic abnormality) [SNOMED CT concept]
- Congenital malformation (disorder) [SNOMED CT concept]
- Congenital malformation (morphologic abnormality) [Inactive SNOMED CT concept]
- Congenital malformation, unspecified [ICD-10 Sub-category]
- Developmental anomaly (morphologic abnormality) [SNOMED CT concept]
- Developmental disturbance [MedDRA LLT]
- Fetal anomaly [HPO term]
- Fetal malformation [MedDRA LLT]
- Foetal malformation [MedDRA Preferred Term]
- congenital abnormalities [MeSH Descriptor]
- congenital abnormalities [MeSH concept]
- developmental anomaly, nos [SNOMED Notion]

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