pentalogy of Cantrell
disease
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pentalogy of Cantrell
Summary
pentalogy of Cantrell is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- pentalogy of Cantrell's instance of is recorded as developmental defect during embryogenesis[3].
- pentalogy of Cantrell's instance of is recorded as class of disease[4].
- pentalogy of Cantrell is a type of congenital disorder[5].
- pentalogy of Cantrell is a type of rare genetic developmental defect during embryogenesis[6].
- pentalogy of Cantrell is a type of syndromic diaphragmatic or abdominal wall malformation[7].
- pentalogy of Cantrell is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[8].
- pentalogy of Cantrell is a type of syndromic diaphragmatic or thoracic malformation[9].
- pentalogy of Cantrell's Commons category is recorded as Pentalogy of Cantrell[10].
- pentalogy of Cantrell's time of discovery or invention is recorded as 1958[11].
- pentalogy of Cantrell's symptoms and signs is recorded as omphalocele[12].
- pentalogy of Cantrell's symptoms and signs is recorded as diaphragmatic hernia[13].
- pentalogy of Cantrell's symptoms and signs is recorded as ectopia cordis[14].
- pentalogy of Cantrell's symptoms and signs is recorded as Sternal cleft[15].
- pentalogy of Cantrell's ICD-9-CM is recorded as 759.89[16].
- pentalogy of Cantrell's NCI Thesaurus ID is recorded as C99011[17].
- pentalogy of Cantrell's health specialty is recorded as medical genetics[18].
- pentalogy of Cantrell's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1335[19].
Why It Matters
pentalogy of Cantrell has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 13 alternative names across languages and contexts.[20]