Denys-Drash syndrome
Human disease
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Summary
Denys-Drash syndrome is a rare disease[1]. It draws 209 Wikipedia views per month (rare disease category, ranking #114 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Named after: Pierre Denys[4], Allan L. Drash[5]
- Subclass of: autosomal dominant disease[6], nephroblastoma[7], pseudohermaphroditism[8], primary glomerular disease[9], syndrome with disorder of sex development of gynecological interest[10], polymalformative genetic syndrome with increased risk of developing cancer[11], syndrome with 46,XY disorder of sex development[12], syndrome[13], developmental defect during embryogenesis[14]
- ICD-9-CM: 189.0[15]
- NCI Thesaurus ID: C84668[16]
- Health specialty: oncology[17], endocrinology[18], urology[19], obstetrics and gynaecology[20], medical genetics[21]
- Genetic association: WT1[22]
- Exact match: http://purl.obolibrary.org/obo/DOID_3764[23], http://identifiers.org/doid/DOID:3764[24], http://www.orpha.net/ORDO/Orphanet_220[25]
- On focus list of Wikimedia project: WikiProject Medicine[26]
Why It Matters
Denys-Drash syndrome has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[27] It is known by 19 alternative names across languages and contexts.[28]