Q99.9 CHROMOSOMAL ABNORMALITY, UNSPECIFIED

Synonyms

• Alpha-thalassemia intellectual disability syndrome linked to chromosome 16
• Anomaly of chromosome pair 1
• Anomaly of chromosome pair 10
• Anomaly of chromosome pair 11
• Anomaly of chromosome pair 12
• Anomaly of chromosome pair 13
• Anomaly of chromosome pair 14
• Anomaly of chromosome pair 15
• Anomaly of chromosome pair 16
• Anomaly of chromosome pair 17
• Anomaly of chromosome pair 18
• Anomaly of chromosome pair 19
• Anomaly of chromosome pair 2
• Anomaly of chromosome pair 20
• Anomaly of chromosome pair 21
• Anomaly of chromosome pair 22
• Anomaly of chromosome pair 3
• Anomaly of chromosome pair 4
• Anomaly of chromosome pair 5
• Anomaly of chromosome pair 6
• Anomaly of chromosome pair 7
• Anomaly of chromosome pair 8
• Anomaly of chromosome pair 9
• Autoimmune lymphoproliferative syndrome
• Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
• Autosomal chromosomal disorder
• Autosomal dominant hereditary disorder
• Autosomal hereditary disorder
• Autosomal recessive hereditary disorder
• Autosomal translocation
• Cardiac arrhythmia associated with genetic disorder
• CFTR-related disorder
• Chromosomal disorder
• Congenital chromosomal disease
• Deletion of part of short arm of chromosome 16
• Dementia due to chromosomal anomaly
• Dementia due to genetic disease
• Dominant autosomal hereditary disorder, complete penetrance
• Dominant autosomal hereditary disorder, incomplete penetrance
• Genetic disease
• Immunodeficiency associated with chromosomal abnormality
• Ulnar mammary syndrome

Crosswalk Information

ICD-10 Code		ICD-9 Code	ICD-9 Description
Q99.9		758.9	Chromosome anomaly NOS

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