Concept information
Preferred term
Anomaly of chromosome X
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- 49,XXXYY syndrome
- Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)
- Atypical Norrie disease due to monosomy Xp11.3 (disorder)
- Choroideremia with deafness and obesity syndrome (disorder)
- Chromosome Xp11.3 microdeletion syndrome (disorder)
- Chromosome Xp22.3 microdeletion syndrome (disorder)
- Chromosome Xq27.3q28 duplication syndrome (disorder)
- Intellectual disability, seizures, macrocephaly, obesity syndrome (disorder)
- Klinefelter syndrome
- Microduplication Xp11.22p11.23 syndrome (disorder)
- Paternal uniparental disomy of chromosome X
- Trisomy Xq28 syndrome
- Turner syndrome
- UPD(X)mat - maternal uniparental disomy of chromosome X
- X-linked diffuse leiomyomatosis with Alport syndrome (disorder)
- Xp22.13p22.2 duplication syndrome
- Xq12-q13.3 duplication syndrome (disorder)
- X small rings
Associated morphology
Finding site
Occurrence
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/111312006
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