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DO Term : lissencephaly [DOID:0050453] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
SNOMEDCT_US_2023_03_01:204036008,
ICD10CM:Q04.3,
OMIM:PS607432,
UMLS_CUI:C0266483,
MESH:D054082,
ORDO:102009,
NCI:C103921,
PS607432,
SNOMEDCT_US_2023_03_01:23024003,
UMLS_CUI:C0266463,
GARD:12291

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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