Preferred Name |
Schizencephaly |
|
Synonyms |
|
|
Definitions |
The presence of a cleft in the cerebral cortex unilaterally or bilaterally, usually located in the frontal area. |
|
ID |
http://purl.obolibrary.org/obo/HP_0010636 |
|
created_by |
peter |
|
creation_date |
2009-12-06T08:05:54Z |
|
database_cross_reference |
SNOMEDCT_US:253159001 UMLS:C0266484 MSH:D065707 SNOMEDCT_US:38353004 |
|
fromILAE |
true |
|
has_obo_namespace |
human_phenotype |
|
hasDefinition |
Schizencephaly is an uncommon malformation of cortical development that results in a cleft, lined by polymicrogyria, that extends from the ependyma of the ventricles to the pia mater. The majority of clefts are posterior frontal or parietal, but temporal or occipital location can occur. |
|
id |
HP:0010636 |
|
imported from | ||
label |
Schizencephaly |
|
notation |
HP:0010636 |
|
prefLabel |
Schizencephaly |
|
文本定义 |
The presence of a cleft in the cerebral cortex unilaterally or bilaterally, usually located in the frontal area. |
|
subClassOf |
Create mapping