46, XX/XY
human disease
Facts
5 properties- Instance of
- rare disease, intersex, class of disease[2][3]
- Subclass of
- chimera, sex chromosome disorder of sex development, syndrome with disorder of sex development of gynecological interest, sex chromosome disorder, developmental defect during embryogenesis[4][5][6][7][8]
- Has phenotype
- cryptorchidism, Perineal hypospadias, micropenis, disorder of sex development, ovarian disease, Hypopigmented skin patches, clitoromegaly, ovotesticular disorder of sex development, Abnormality of multiple cell lineages in the bone marrow[12][13][14][15][16][17][18][19][20]
- On focus list of Wikimedia project
- concrete/abstract disjunction anomalies[11]
🏷️ Also known as
en 46,XX/46,XY chimerism
en 46, XX/XY
en Tetragametic chimerism
fr chimère 46,XX/46,XY
fr chimère tétragamétique
nl 46,XX/46,XY
🔖 Identifiers · 10
- Exact match
- www.orpha.net
- ICD-10 ID
- Q99.0
- ICD-10-CM
- Q99.0
- ICD-11 ID (Foundation)
- 1262245334
- ICD-11 ID (MMS)
- LD56
- Microsoft Academic ID (discontinued)
- 2777500643
- Mondo ID
- MONDO_0016045
- Orphanet ID
- 199310
- Raras disease ID
- D199310
- UMLS CUI
- C5679592
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Summary
46, XX/XY is a rare disease[1].