Marshall syndrome
medical condition
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Marshall syndrome
Summary
Marshall syndrome is a developmental defect during embryogenesis[1]. It draws 21 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's subclass of is recorded as reactive neutrophilic dermatose[7].
- Marshall syndrome's subclass of is recorded as syndromic myopia[8].
- Marshall syndrome's subclass of is recorded as syndromic glaucoma[9].
- Marshall syndrome's subclass of is recorded as syndromic developmental defect of the eye[10].
- Marshall syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability[11].
- Marshall syndrome's subclass of is recorded as type 11 collagen-related bone disorder[12].
- Marshall syndrome's Commons category is recorded as Marshall syndrome[13].
- Marshall syndrome's MeSH descriptor ID is recorded as C536025[14].
- Marshall syndrome's OMIM ID is recorded as 154780[15].
- Marshall syndrome's ICD-10 ID is recorded as Q87.0[16].
- Marshall syndrome's DiseasesDB is recorded as 31965[17].
- Marshall syndrome's KEGG ID is recorded as H02081[18].
- Marshall syndrome's Orphanet ID is recorded as 560[19].
- Marshall syndrome's ICD-9-CM is recorded as 759.89[20].
- Marshall syndrome's NCI Thesaurus ID is recorded as C128115[21].
- Marshall syndrome's different from is recorded as periodic fever, aphthous stomatitis, pharyngitis and adenitis[22].
- Marshall syndrome's genetic association is recorded as COL11A1[23].
- Marshall syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_560[24].
- Marshall syndrome's UMLS CUI is recorded as C0265235[25].
- Marshall syndrome's ICD-10-CM is recorded as Q87.0[26].
- Marshall syndrome's GARD rare disease ID is recorded as 6984[27].
Why It Matters
Marshall syndrome draws 21 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.[28] It is known by 3 alternative names across languages and contexts.[29]