Norman–Roberts syndrome
lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.
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Norman–Roberts syndrome
Summary
Norman–Roberts syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Norman–Roberts syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Norman–Roberts syndrome's instance of is recorded as rare disease[4].
- Norman–Roberts syndrome's instance of is recorded as class of disease[5].
- Norman–Roberts syndrome is a type of syndromic lymphedema[6].
- Norman–Roberts syndrome is a type of rare genetic immune disease[7].
- Norman–Roberts syndrome is a type of primary lymphedema with associated anomalies[8].
- Norman–Roberts syndrome is a type of genetic vascular anomaly[9].
- Norman–Roberts syndrome is a type of Microlissencephaly[10].
- Norman–Roberts syndrome is a type of lissencephaly[11].
- Norman–Roberts syndrome is a type of genetic disease[12].
- Norman–Roberts syndrome is a type of autosomal recessive disease[13].
- Norman–Roberts syndrome's health specialty is recorded as medical genetics[14].
- Norman–Roberts syndrome's genetic association is recorded as RELN[15].
- Norman–Roberts syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060902[16].
- Norman–Roberts syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060902[17].
- Norman–Roberts syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_89844[18].
- Norman–Roberts syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Norman–Roberts syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[20]