Char syndrome
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Char syndrome
Summary
Char syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[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 is a type of patent ductus arteriosus[7].
- Char syndrome is a type of ptosis[8].
- Char syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[9].
- Char syndrome's ICD-9-CM is recorded as 759.89[10].
- Char syndrome's health specialty is recorded as medical genetics[11].
- Char syndrome's genetic association is recorded as TFAP2B[12].
- Char syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060563[13].
- Char syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060563[14].
- Char syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_46627[15].
- Char syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Char syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 3 alternative names across languages and contexts.[17]