Nijmegen breakage syndrome

Summary

Nijmegen breakage syndrome is a developmental defect during embryogenesis^[1]. It draws 16 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #120 of 308).^[2]

Key Facts

• Nijmegen breakage syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Nijmegen breakage syndrome's instance of is recorded as rare disease^[4].
• Nijmegen breakage syndrome's instance of is recorded as class of disease^[5].
• Nijmegen is named after Nijmegen breakage syndrome^[6].
• Nijmegen breakage syndrome's subclass of is recorded as autosomal recessive disease^[7].
• Nijmegen breakage syndrome's subclass of is recorded as inherited tumor^[8].
• Nijmegen breakage syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[9].
• Nijmegen breakage syndrome's subclass of is recorded as developmental anomaly of metabolic origin^[10].
• Nijmegen breakage syndrome's subclass of is recorded as DNA repair defect other than combined T-cell and B-cell immunodeficiencies^[11].
• Nijmegen breakage syndrome's subclass of is recorded as rare genetic developmental defect during embryogenesis^[12].
• Nijmegen breakage syndrome's subclass of is recorded as polymalformative genetic syndrome with increased risk of developing cancer^[13].
• Nijmegen breakage syndrome's subclass of is recorded as syndrome^[14].
• Nijmegen breakage syndrome's MeSH descriptor ID is recorded as D049932^[15].
• Nijmegen breakage syndrome's OMIM ID is recorded as 251260^[16].
• Nijmegen breakage syndrome's DiseasesDB is recorded as 32395^[17].
• Nijmegen breakage syndrome's Freebase ID is recorded as /m/09wrvw^[18].
• Nijmegen breakage syndrome's KEGG ID is recorded as H01344^[19].
• Nijmegen breakage syndrome's GeneReviews ID is recorded as NBK1176^[20].
• Nijmegen breakage syndrome's MeSH tree code is recorded as C18.452.284.600^[21].
• Nijmegen breakage syndrome's Disease Ontology ID is recorded as DOID:7400^[22].
• Nijmegen breakage syndrome's Orphanet ID is recorded as 647^[23].
• Nijmegen breakage syndrome's NCI Thesaurus ID is recorded as C4692^[24].
• Nijmegen breakage syndrome's health specialty is recorded as endocrinology^[25].
• Nijmegen breakage syndrome's genetic association is recorded as NBN^[26].
• Nijmegen breakage syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_7400^[27].

Why It Matters

Nijmegen breakage syndrome draws 16 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #120 of 308).^[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.^[28] It is known by 25 alternative names across languages and contexts.^[29]