Marshall syndrome
medical condition
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Marshall syndrome
Summary
Marshall syndrome is a developmental defect during embryogenesis[1]. It draws 19 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #121 of 308).[2]
Key Facts
- Marshall syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Marshall syndrome's instance of is recorded as rare disease[4].
- Marshall syndrome's instance of is recorded as class of disease[5].
- Don Marshall is named after Marshall syndrome[6].
- Marshall syndrome is a type of reactive neutrophilic dermatose[7].
- Marshall syndrome is a type of syndromic myopia[8].
- Marshall syndrome is a type of syndromic glaucoma[9].
- Marshall syndrome is a type of syndromic developmental defect of the eye[10].
- Marshall syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[11].
- Marshall syndrome is a type of type 11 collagen-related bone disorder[12].
- Marshall syndrome's Commons category is recorded as Marshall syndrome[13].
- Marshall syndrome's ICD-9-CM is recorded as 759.89[14].
- Marshall syndrome's NCI Thesaurus ID is recorded as C128115[15].
- Marshall syndrome's different from is recorded as periodic fever, aphthous stomatitis, pharyngitis and adenitis[16].
- Marshall syndrome's genetic association is recorded as COL11A1[17].
- Marshall syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_560[18].
Why It Matters
Marshall syndrome draws 19 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #121 of 308).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[19] It is known by 3 alternative names across languages and contexts.[20]