Warsaw breakage syndrome
Human disease
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Summary
Warsaw breakage syndrome is a developmental defect during embryogenesis[1]. It draws 98 Wikipedia views per month (developmental defect during embryogenesis category, ranking #132 of 308).[2]
Key Facts
- Instance of: rare disease[3], class of disease[4]
- Subclass of: syndrome[5], inherited tumor[6], rare genetic developmental defect during embryogenesis[7], multiple congenital anomalies/dysmorphic syndrome without intellectual disability[8], polymalformative genetic syndrome with increased risk of developing cancer[9], genetic disease[10], autosomal recessive disease[11]
- ICD-9-CM: 759.89[12]
- NCI Thesaurus ID: C164675[13]
- Genetic association: DDX11[14]
- Exact match: http://purl.obolibrary.org/obo/DOID_0060535[15], http://identifiers.org/doid/DOID:0060535[16], http://www.orpha.net/ORDO/Orphanet_280558[17]
- On focus list of Wikimedia project: WikiProject Medicine[18]
Why It Matters
Warsaw breakage syndrome is known by 5 alternative names across languages and contexts.[19]