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PMO Precision Medicine Ontology
Last uploaded:
December 16, 2020
| Id | http://www.phoc.org.cn/pmo/class/PMO_00085540
http://www.phoc.org.cn/pmo/class/PMO_00085540
|
|---|---|
| Preferred Name | Lissencephaly |
| 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.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | Lissencephaly
|
|---|---|
| label | Lissencephaly
|
| 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.
|
| Tree Number |
T9.21.16.2.2.1
T9.8.3.20.2.2.1
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| type | |
| Synonym |
Lissencephaly [Disease/Finding]
lissencephaly (diagnosis)
Lissencephalia
Lissencephaly pachygyria
Lissencephalies
Pachygyria/lissencephaly
Lissencephaly (disorder)
lissencephaly
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| MCID | MC00091102
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| prefixIRI | pmo:PMO_00085540
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| PMOID | PMO:00085540
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| Database_Cross_Reference |
HPO:HP:0001339
ICD10CM:Q04.3
MTH:NOCODE
NCI_NICHD:C103921
DO:DOID:0050453
RCD:P223.
NDFRT:N0000181090
SNM:M-25440
OMIM:MTHU037613
MSH:D054082
LCH_NW:sh00010142
MEDCIN:218978
SNOMEDCT_US:204036008
NCI:C103921
MDR:10048911
CHV:0000026051
OMIM:MTHU050742
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| subClassOf |
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