XXXY syndrome
chromosomal anomaly of the aneuploidic type characterized by the presence of two extra X chromosomes in males
Press Enter · cited answer in seconds
0 sources
XXXY syndrome
Summary
XXXY syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- XXXY syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- XXXY syndrome's instance of is recorded as class of disease[4].
- XXXY syndrome is a type of chromosomal disease[5].
- XXXY syndrome is a type of sex chromosome disorder[6].
- XXXY syndrome is a type of X chromosome number anomaly with male phenotype[7].
- XXXY syndrome is a type of male infertility due to gonadal dysgenesis[8].
- XXXY syndrome is a type of genetic syndromic intellectual disability[9].
- XXXY syndrome is a type of sex chromosome disorder of sex development[10].
- XXXY syndrome is a type of syndromic urogenital tract malformation[11].
- XXXY syndrome's Commons category is recorded as XXXY syndrome[12].
- XXXY syndrome's ICD-9-CM is recorded as 758.81[13].
- XXXY syndrome's NCI Thesaurus ID is recorded as C89799[14].
- XXXY syndrome's different from is recorded as XXYYY syndrome[15].
- XXXY syndrome's different from is recorded as 49,XXXYY syndrome[16].
- XXXY syndrome's different from is recorded as XXYY syndrome[17].
- XXXY syndrome's different from is recorded as 49,XXXXY syndrome[18].
- XXXY syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_96263[19].
Why It Matters
XXXY syndrome has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2] It is known by 4 alternative names across languages and contexts.[20]