OBO ID: DOID:0112235 |
Term Name: | lissencephaly 4 | Search Ontology: | |
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Definition: | A microlissencephaly characterized by lissencephaly, severe brain atrophy, extreme microcephaly, and profound intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the NDE1 gene on chromosome 16p13.11. (2) | ||
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Ontology: | Human Disease ( DOID:0112235 ) |
OTHER lissencephaly 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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