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Drug Target Ontology
Last uploaded:
February 15, 2018
| 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. |
|---|---|
| prefLabel | lissencephaly
|
| label | lissencephaly
|
| comment | Xref MGI.
OMIM mapping confirmed by DO. [SN].
|
| hasOBONamespace | disease_ontology
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| type | |
| imported from | |
| id | DOID:0050453
|
| prefixIRI | DOID:0050453
|
| hasDbXref |
MESH:D054082
ICD10CM:Q04.3
OMIM:300215
OMIM:611603
ORDO:102009
OMIM:300067
ICD10CM:Q04.8
SNOMEDCT_US_2016_03_01:204036008
OMIM:615191
UMLS_CUI:C0266463
OMIM:614019
SNOMEDCT_US_2016_03_01:23024003
OMIM:607432
UMLS_CUI:C0266483
NCI:C103921
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| inSubset | |
| subClassOf |
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