Nijmegen breakage syndrome
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Nijmegen breakage syndrome
Summary
Nijmegen breakage syndrome is a developmental defect during embryogenesis[1]. It draws 29 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 is a type of autosomal recessive disease[7].
- Nijmegen breakage syndrome is a type of inherited tumor[8].
- Nijmegen breakage syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[9].
- Nijmegen breakage syndrome is a type of developmental anomaly of metabolic origin[10].
- Nijmegen breakage syndrome is a type of DNA repair defect other than combined T-cell and B-cell immunodeficiencies[11].
- Nijmegen breakage syndrome is a type of rare genetic developmental defect during embryogenesis[12].
- Nijmegen breakage syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer[13].
- Nijmegen breakage syndrome is a type of syndrome[14].
- Nijmegen breakage syndrome's NCI Thesaurus ID is recorded as C4692[15].
- Nijmegen breakage syndrome's health specialty is recorded as endocrinology[16].
- Nijmegen breakage syndrome's genetic association is recorded as NBN[17].
- Nijmegen breakage syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_7400[18].
- Nijmegen breakage syndrome's exact match is recorded as http://identifiers.org/doid/DOID:7400[19].
- Nijmegen breakage syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_647[20].
- Nijmegen breakage syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
Nijmegen breakage syndrome draws 29 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.[22] It is known by 25 alternative names across languages and contexts.[23]