Malformaciones del Desarrollo Cortical - CISMeF

CISMeF

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Malformaciones del Desarrollo CorticalDescripteur MeSH

Preferred Label : Malformaciones del Desarrollo Cortical;

Details

Origin ID

D054220;

UMLS CUI

C1955869;

Automatic exact mappings (from CISMeF team)
- Disgenesia cortical cerebral [MedDRA LLT]
- Displasia cortical [MedDRA Preferred Term]
- Displasia cortical focal [MedDRA LLT]
- Displasia cortical focal aislada [ORDO Disease]
- Esquizencefalia [ORDO Disease]
- Esquizencefalia [HRDO Sign]
- Esquizencefalia [MedDRA Preferred Term]
- Megalencefalia [ORDO Disease]
- Megalencefalia [HRDO Sign]
- Megalencefalia unilateral [ORDO Disease]
- Polimicrogiria [MedDRA Preferred Term]
- Polimicrogiria [ORDO Disease]
- disgenesia cerebral cortical (trastorno) [Concepto SNOMED CT]
- displasia cortical (trastorno) [Concepto SNOMED CT]
- displasia cortical del cerebelo (trastorno) [Concepto SNOMED CT]
- displasia de corteza cerebral [Concepto SNOMED CT inactivo]
- esquizoencefalia (trastorno) [Concepto SNOMED CT]
- hemimegalencefalia (trastorno) [Concepto SNOMED CT]
- microgiria (trastorno) [Concepto SNOMED CT]
- porencefalia congénita (trastorno) [Concepto SNOMED CT]
Manual BTNT mappings - CISMeF
- Polimicrogiria bilateral frontoparietal [ORDO Disease]
- Polimicrogiria bilateral perisilviana [ORDO Disease]
- Polimicrogiria frontal bilateral [ORDO Disease]
- Polimicrogiria generalizada bilateral [ORDO Disease]
- Polimicrogiria parietooccipital parasagital bilateral [ORDO Disease]
- Polimicrogiria unilateral hemisférica [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Discapacidad intelectual rara genética sindrómica [ORDO Disease]
- Discapacidad intelectual rara sindrómica [ORDO Disease]
- Malformación cerebral con epilepsia [ORDO Disease]
- Malformación del vermis cerebeloso [ORDO Disease]
- Malformación no sindrómica del sistema nervioso central [ORDO Disease]
See also (suggested by CISMeF)
- Corteza Cerebral [MeSH Descriptor]

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18/06/2025

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