Char syndrome
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Char syndrome
Summary
Char syndrome is a developmental defect during embryogenesis[1]. It draws 29 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #109 of 308).[2]
Key Facts
- Char syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Char syndrome's instance of is recorded as congenital disorder[4].
- Char syndrome's instance of is recorded as rare disease[5].
- Char syndrome's instance of is recorded as class of disease[6].
- Char syndrome's subclass of is recorded as patent ductus arteriosus[7].
- Char syndrome's subclass of is recorded as ptosis[8].
- Char syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[9].
- Char syndrome's MeSH descriptor ID is recorded as C566815[10].
- Char syndrome's OMIM ID is recorded as 169100[11].
- Char syndrome's ICD-10 ID is recorded as Q87.8[12].
- Char syndrome's KEGG ID is recorded as H00555[13].
- Char syndrome's GeneReviews ID is recorded as NBK1106[14].
- Char syndrome's Disease Ontology ID is recorded as DOID:0060563[15].
- Char syndrome's Orphanet ID is recorded as 46627[16].
- Char syndrome's ICD-9-CM is recorded as 759.89[17].
- Char syndrome's health specialty is recorded as medical genetics[18].
- Char syndrome's genetic association is recorded as TFAP2B[19].
- Char syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060563[20].
- Char syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060563[21].
- Char syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_46627[22].
- Char syndrome's UMLS CUI is recorded as C1868570[23].
- Char syndrome's ICD-10-CM is recorded as Q87.8[24].
- Char syndrome's GARD rare disease ID is recorded as 1237[25].
- Char syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[26].
- Char syndrome's Mondo ID is recorded as MONDO_0008209[27].
Why It Matters
Char syndrome draws 29 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #109 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]