2013 ICD-9-CM Diagnosis Code 758.5
Other conditions due to autosomal anomalies
- Short description: Autosomal anomalies NEC.
- ICD-9-CM 758.5 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.5 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2013 version of ICD-9-CM 758.5.
- More recent version(s) of ICD-9-CM 758.5: 2014 2015.
Convert to ICD-10-CM:
758.5 converts approximately to:
- 2015/16 ICD-10-CM Q92.8 Other specified trisomies and partial trisomies of autosomes
Approximate Synonyms
- 10p partial trisomy syndrome
- 10q partial trisomy syndrome
- 11p partial trisomy syndrome
- 11q partial trisomy syndrome
- 12p partial trisomy syndrome
- 12q partial trisomy syndrome
- 15q partial trisomy syndrome
- 16q partial trisomy syndrome
- 17p partial trisomy syndrome
- 17q partial trisomy syndrome
- 19q partial trisomy syndrome
- 1q partial trisomy syndrome
- 20p partial trisomy syndrome
- 20q partial trisomy syndrome
- 2q partial trisomy syndrome
- 3p partial trisomy syndrome
- 3q partial trisomy syndrome
- 4p partial trisomy syndrome
- 4q partial trisomy syndrome
- 5p partial trisomy syndrome
- 6p partial trisomy syndrome
- 6q partial trisomy syndrome
- 7p partial trisomy syndrome
- 7q partial trisomy syndrome
- 8p partial trisomy syndrome
- 8q partial trisomy syndrome
- 9p partial trisomy syndrome
- 9q partial trisomy syndrome
- Autosomal aneuploidy
- Autosomal anomaly
- AUTOSOMAL ANOMALY (disorder)
- Autosomal chromosomal disorder
- Autosomal deletion - mosaicism
- Autosomal dominant hereditary disorder
- Autosomal duplication
- Autosomal hereditary disorder
- Autosomal recessive hereditary disorder
- Complete trisomy 10 syndrome
- Complete trisomy 20 syndrome
- Complete trisomy 8 syndrome
- Complete trisomy 9 syndrome
- Dominant autosomal hereditary disorder, complete penetrance
- Dominant autosomal hereditary disorder, incomplete penetrance
- Individual with autosomal fragile site
- Major partial trisomy
- Partial trisomy syndromes
- Pyle metaphyseal dysplasia
- Trisomy 10
- Trisomy 11
- Trisomy 12
- Trisomy 6
- Trisomy 7
- Trisomy 8
- Trisomy 9
- Trisomy and partial trisomy of autosome
- Unbalanced translocation and insertion
- Whole chromosome trisomy - meiotic nondisjunction
- Whole chromosome trisomy - mitotic nondisjunction mosaicism
ICD-9-CM Volume 2 Index entries containing back-references to
758.5:
- Abnormal, abnormality, abnormalities - see also Anomaly
- autosomes NEC 758.5
- chromosomal NEC 758.89
- analysis, nonspecific result 795.2
- autosomes (see also Abnormal, autosomes NEC) 758.5
- fetal, (suspected) affecting management of pregnancy 655.1
- sex 758.81
- Accessory (congenital)
- autosome(s) NEC 758.5
- chromosome(s) NEC 758.5
- Additional - see also Accessory
- chromosome(s) 758.5
- Aneuploidy NEC 758.5
- Anomaly, anomalous (congenital) (unspecified type) 759.9
- autosomes, autosomal NEC 758.5
- chromosomes, chromosomal 758.9
- Mosaicism, mosaic (chromosomal) 758.9
- autosomal 758.5
- Syndrome - see also Disease
- due to abnormality
- autosomal NEC (see also Abnormal, autosomes NEC) 758.5
- chromosomal 758.89
- trisomy NEC 758.5
- Translocation
- autosomes NEC 758.5
- Trisomy (syndrome) NEC 758.5
- autosomes NEC 758.5