FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term lissencephaly ID (Ontology) DOID:0050453 (Human Disease)
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.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       2
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 lissencephaly       2      1      1
 model of | lissencephaly       2       --       --
Spanning Tree (Parents/Children)
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physical disorder_______
nervous system disease__|
                        congenital nervous system abnormality
                         |__lissencephaly  21 rec.
                             |__lissencephaly 1 1 rec.
                             |__lissencephaly 3 4 rec.
                             |__lissencephaly 5 1 rec.
                             |__lissencephaly 7 with cerebellar hypoplasia 1 rec.
                             |__lissencephaly 8 2 rec.
                             |__lissencephaly 9 with complex brainstem malformation 1 rec.
                             |__lissencephaly 10
                             |__microlissencephaly 3 rec.
                             |   |__lissencephaly 4 1 rec.
                             |   |__lissencephaly 6 2 rec.
                             |__Norman-Roberts syndrome
                             |__X-linked lissencephaly 1 1 rec.
                             |__X-linked lissencephaly 2 3 rec.
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Is a congenital nervous system abnormality
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GARD:12291
ICD10CM:Q04.3
MESH:D054082
MIM:PS607432
NCI:C103921
ORDO:102009
SNOMEDCT_US_2023_03_01:204036008
SNOMEDCT_US_2023_03_01:23024003
UMLS_CUI:C0266463
UMLS_CUI:C0266483