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bn:15670519n
Noun Concept
Categories: Rare syndromes, Neurological disorders, Congenital disorders
EN
Norman–Roberts syndrome  lissencephaly 2  LIS2  LISSENCEPHALY 2; LIS2  lissencephaly syndrome, Norman-Roberts type
EN
Norman–Roberts syndrome is a rare form of microlissencephaly caused by a mutation in the RELN gene. Wikipedia
Definitions
Relations
Sources
EN
Norman–Roberts syndrome is a rare form of microlissencephaly caused by a mutation in the RELN gene. Wikipedia
Lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22. Wikidata
IS A
rare disease
genetic disease
lissencephaly
autosomal recessive disease
microlissencephaly
GENETIC ASSOCIATION
reelin
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
Norman–Roberts syndrome
Wikidata
EN
Norman–Roberts syndrome
Wikipedia Redirections
EN
LIS2, Lissencephaly 2, Norman-Roberts lissencephaly syndrome, Norman-Roberts syndrome, Norman Roberts lissencephaly syndrome, Norman–Roberts lissencephaly syndrome
Wikidata Alias
EN
LIS2, lissencephaly 2, Lissencephaly 2, LISSENCEPHALY 2; LIS2, lissencephaly syndrome, Norman-Roberts type, Lissencephaly type 2, Microlissencephaly type A, Norman-Roberts syndrome

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