schizencephaly
rare birth defect characterized by abnormal clefts lined with grey matter that form the ependyma of the cerebral ventricles to the pia mater.
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schizencephaly
Summary
schizencephaly is a developmental defect during embryogenesis[1]. schizencephaly has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- schizencephaly's instance of is recorded as developmental defect during embryogenesis[3].
- schizencephaly's instance of is recorded as rare disease[4].
- schizencephaly's instance of is recorded as class of disease[5].
- schizencephaly is a type of malformations of cortical development, Group III[6].
- schizencephaly is a type of Encephaloclastic disorder[7].
- schizencephaly is a type of cerebral malformation with epilepsy[8].
- schizencephaly's Commons category is recorded as Schizencephaly[9].
- schizencephaly's ICD-9-CM is recorded as 742.4[10].
- schizencephaly's NCI Thesaurus ID is recorded as C99056[11].
- schizencephaly's health specialty is recorded as medical genetics[12].
- schizencephaly's health specialty is recorded as neurology[13].
- schizencephaly's genetic association is recorded as SIX3[14].
- schizencephaly's genetic association is recorded as EMX2[15].
- schizencephaly's genetic association is recorded as COL4A1[16].
- schizencephaly's genetic association is recorded as SHH[17].
- schizencephaly's exact match is recorded as http://purl.obolibrary.org/obo/HP_0010636[18].
- schizencephaly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_799[19].
Why It Matters
schizencephaly has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]