OBO ID: DOID:0060902
Term Name: Norman-Roberts syndrome Search Ontology:
Synonyms:
  • lissencephaly 2
  • lissencephaly syndrome, Norman-Roberts type
Definition: A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22. (2)
References:
Ontology: Human Disease   ( DOID:0060902 )
Relationships
is a type of:
OTHER Norman-Roberts syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RELN Lissencephaly 2 (Norman-Roberts type) 257320
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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