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. |
|
| ID |
http://www.phoc.org.cn/pmo/class/PMO_00085540 |
|
| 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 |
|
| 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 |
|
| MCID |
MC00091102 |
|
| PMOID |
PMO:00085540 |
|
| prefixIRI |
pmo:PMO_00085540 |
|
| prefLabel |
Lissencephaly |
|
| Synonym |
Lissencephaly [Disease/Finding] lissencephaly (diagnosis) Lissencephalia Lissencephaly pachygyria Lissencephalies Pachygyria/lissencephaly Lissencephaly (disorder) lissencephaly |
|
| Tree Number |
T9.21.16.2.2.1 T9.8.3.20.2.2.1 |
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| subClassOf |