48,XXXX syndrome
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48,XXXX syndrome
Summary
48,XXXX syndrome is a rare disease[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- 48,XXXX syndrome's instance of is recorded as rare disease[3].
- 48,XXXX syndrome's instance of is recorded as chromosomal disease[4].
- 48,XXXX syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- 48,XXXX syndrome's instance of is recorded as class of disease[6].
- 48,XXXX syndrome is a type of tetrasomy[7].
- 48,XXXX syndrome is a type of sex chromosome disorder[8].
- 48,XXXX syndrome is a type of non-acquired premature ovarian failure[9].
- 48,XXXX syndrome is a type of rare female infertility due to an anomaly of ovarian function of genetic origin[10].
- 48,XXXX syndrome is a type of polysomy of X chromosome[11].
- 48,XXXX syndrome's Commons category is recorded as Tetrasomy X[12].
- 48,XXXX syndrome's ICD-9-CM is recorded as 758.81[13].
- 48,XXXX syndrome's health specialty is recorded as medical genetics[14].
Why It Matters
48,XXXX syndrome has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 17 alternative names across languages and contexts.[15]