Pallister–Killian syndrome
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Pallister–Killian syndrome
Summary
Pallister–Killian syndrome is a rare disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Pallister–Killian syndrome's instance of is recorded as rare disease[3].
- Pallister–Killian syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Pallister–Killian syndrome's instance of is recorded as class of disease[5].
- Philip David Pallister is named after Pallister–Killian syndrome[6].
- Maria Teschler-Nicola is named after Pallister–Killian syndrome[7].
- Pallister–Killian syndrome is a type of tetrasomy[8].
- Pallister–Killian syndrome is a type of syndromic diaphragmatic or thoracic malformation[9].
- Pallister–Killian syndrome is a type of chromosomal anomaly with epilepsy as a major feature[10].
- Pallister–Killian syndrome is a type of chromosomal disease with overgrowth[11].
- Pallister–Killian syndrome is a type of syndromic diaphragmatic or abdominal wall malformation[12].
- Pallister–Killian syndrome is a type of syndromic anorectal malformation[13].
- Pallister–Killian syndrome is a type of partial trisomy/tetrasomy of the short arm of chromosome 12[14].
- Pallister–Killian syndrome's Commons category is recorded as Pallister–Killian syndrome[15].
- Pallister–Killian syndrome's symptoms and signs is recorded as hypotonia[16].
- Pallister–Killian syndrome's symptoms and signs is recorded as developmental language disorder[17].
- Pallister–Killian syndrome's symptoms and signs is recorded as epilepsy[18].
- Pallister–Killian syndrome's symptoms and signs is recorded as polydactyly[19].
- Pallister–Killian syndrome's symptoms and signs is recorded as diaphragmatic hernia[20].
- Pallister–Killian syndrome's ICD-9-CM is recorded as 758.81[21].
- Pallister–Killian syndrome's NCI Thesaurus ID is recorded as C75458[22].
- Pallister–Killian syndrome's health specialty is recorded as medical genetics[23].
- Pallister–Killian syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_884[24].
Why It Matters
Pallister–Killian syndrome has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 21 alternative names across languages and contexts.[25]