triploid syndrome
extremely rare chromosomal disorder occuring during human embryogenesis, causing severe abnormalities in fetal development and usually lethal in the prenatal stage
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triploid syndrome
Summary
triploid syndrome is a developmental defect during embryogenesis[1]. It draws 77 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #61 of 308).[2]
Key Facts
- triploid syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- triploid syndrome's instance of is recorded as class of disease[4].
- triploid syndrome is a type of genetic disease[5].
- triploid syndrome is a type of chromosomal anomaly with cataract[6].
- triploid syndrome is a type of syndromic obesity[7].
- triploid syndrome's has cause is recorded as triploidy[8].
- triploid syndrome's ICD-9-CM is recorded as 758.89[9].
- triploid syndrome's NCI Thesaurus ID is recorded as C85204[10].
- triploid syndrome's health specialty is recorded as medical genetics[11].
- triploid syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3376[12].
Why It Matters
triploid syndrome draws 77 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #61 of 308).[2] It is known by 5 alternative names across languages and contexts.[13]