loading...| Preferred Name | lissencephaly | |
| Synonyms |
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|
| Definitions |
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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0050453 |
|
| comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| database_cross_reference |
MESH:D054082 SNOMEDCT_US_2023_03_01:204036008 ICD10CM:Q04.3 ORDO:102009 UMLS_CUI:C0266483 SNOMEDCT_US_2023_03_01:23024003 MIM:PS607432 NCI:C103921 UMLS_CUI:C0266463 GARD:12291 |
|
| 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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| disease has location | ||
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0050453 |
|
| in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
|
| label |
lissencephaly |
|
| notation |
DOID:0050453 |
|
| note |
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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
| preferred label |
lissencephaly |
|
| prefLabel |
lissencephaly |
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| subClassOf |