Watson syndrome
medical condition
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Watson syndrome
Summary
Watson syndrome is a developmental defect during embryogenesis[1]. It draws 20 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #116 of 308).[2]
Key Facts
- Watson syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Watson syndrome's instance of is recorded as rare disease[4].
- Watson syndrome's instance of is recorded as class of disease[5].
- Watson syndrome's subclass of is recorded as pulmonary valve stenosis[6].
- Watson syndrome's OMIM ID is recorded as 193520[7].
- Watson syndrome's ICD-10 ID is recorded as Q87.1[8].
- Watson syndrome's DiseasesDB is recorded as 32244[9].
- Watson syndrome's Freebase ID is recorded as /m/07k4wpr[10].
- Watson syndrome's KEGG ID is recorded as H02188[11].
- Watson syndrome's Orphanet ID is recorded as 3444[12].
- Watson syndrome's ICD-9-CM is recorded as 709.8[13].
- Watson syndrome's health specialty is recorded as medical genetics[14].
- Watson syndrome's genetic association is recorded as NF1[15].
- Watson syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3444[16].
- Watson syndrome's UMLS CUI is recorded as C0553586[17].
- Watson syndrome's UMLS CUI is recorded as C0347915[18].
- Watson syndrome's GARD rare disease ID is recorded as 5540[19].
- Watson syndrome's Mondo ID is recorded as MONDO_0008672[20].
- Watson syndrome's Microsoft Academic ID is recorded as 2781353584[21].
- Watson syndrome's ICD-11 ID is recorded as 1674178232[22].
- Watson syndrome's UniProt disease ID is recorded as DI-01140[23].
Why It Matters
Watson syndrome draws 20 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #116 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[24] It is known by 6 alternative names across languages and contexts.[25]