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Medical Imaging and Diagnostic Ontology
Last uploaded:
April 25, 2022
| Id | http://purl.obolibrary.org/obo/DOID_0050453
http://purl.obolibrary.org/obo/DOID_0050453
|
|---|---|
| Preferred Name | lissencephaly |
| Definitions |
Xref MGI.
OMIM mapping confirmed by DO. [SN].
A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. |
|---|---|
| label | lissencephaly
|
| prefLabel | lissencephaly
|
| comment | Xref MGI.
OMIM mapping confirmed by DO. [SN].
|
| has_obo_namespace | disease_ontology
|
| id | DOID:0050453
|
| database_cross_reference |
MESH:D054082
ICD10CM:Q04.3
ORDO:102009
SNOMEDCT_US_2021_09_01:204036008
GARD:12291
UMLS_CUI:C0266463
OMIM:PS607432
UMLS_CUI:C0266483
NCI:C103921
SNOMEDCT_US_2021_09_01:23024003
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| in_subset | |
| type | |
| subClassOf | |
| IAO_0000115 | A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.
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| notation | DOID:0050453
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| Delete | Subject | Author | Type | Created |
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