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 draws 6 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #130 of 308).[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's subclass of is recorded as syndromic lymphedema[6].
- Norman–Roberts syndrome's subclass of is recorded as rare genetic immune disease[7].
- Norman–Roberts syndrome's subclass of is recorded as primary lymphedema with associated anomalies[8].
- Norman–Roberts syndrome's subclass of is recorded as genetic vascular anomaly[9].
- Norman–Roberts syndrome's subclass of is recorded as Microlissencephaly[10].
- Norman–Roberts syndrome's subclass of is recorded as lissencephaly[11].
- Norman–Roberts syndrome's subclass of is recorded as genetic disease[12].
- Norman–Roberts syndrome's subclass of is recorded as autosomal recessive disease[13].
- Norman–Roberts syndrome's MeSH descriptor ID is recorded as C537848[14].
- Norman–Roberts syndrome's OMIM ID is recorded as 257320[15].
- Norman–Roberts syndrome's Freebase ID is recorded as /m/03d72kn[16].
- Norman–Roberts syndrome's Disease Ontology ID is recorded as DOID:0060902[17].
- Norman–Roberts syndrome's Orphanet ID is recorded as 89844[18].
- Norman–Roberts syndrome's health specialty is recorded as medical genetics[19].
- Norman–Roberts syndrome's genetic association is recorded as RELN[20].
- Norman–Roberts syndrome's BabelNet ID is recorded as 15670519n[21].
- Norman–Roberts syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060902[22].
- Norman–Roberts syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060902[23].
- Norman–Roberts syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_89844[24].
- Norman–Roberts syndrome's UMLS CUI is recorded as C0796089[25].
- Norman–Roberts syndrome's ICD-10-CM is recorded as Q04.3[26].
- Norman–Roberts syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Norman–Roberts syndrome draws 6 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #130 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 14 alternative names across languages and contexts.[29]