Chromosomal abnormality, NOS: Difference between revisions
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* Chromosomal anomaly | * Chromosomal anomaly | ||
* Genetic disorder | * Genetic disorder | ||
*Edwards syndrome and Patau syndrome | |||
*Chimera 46,XX/46,XY true hermaphrodite | |||
*46,XX true hermaphrodite/46,XX with streak gonads | |||
*46,XY with streak gonads | |||
*46,XY with Pure gonadal dysgenesis | |||
*Fragile X syndrome | |||
*47,XYY | |||
*Klinefelter syndrome | |||
*Cri du chat syndrome | |||
* JAK 2 positivity mutation is a frequent genetic event in the three classical Philadelphia-chromosome negative chronic myeloproliferative disorders (Ph(neg.)- CMPD), polycythemia vera (PV), essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF). Its occurrence varies in frequency in regards to phenotype. | |||
'''Examples''' | '''Examples''' | ||
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**Undescended testicle combine this code with [[Male genital organs NOS, congenital malformation]] | **Undescended testicle combine this code with [[Male genital organs NOS, congenital malformation]] | ||
**Unilateral/Hypospadias, unspecified combine this code with [[Male genital organs NOS, congenital malformation]] | **Unilateral/Hypospadias, unspecified combine this code with [[Male genital organs NOS, congenital malformation]] | ||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||