V19.5 - Family History Of Congenital Anomalies
The ICD 9 Code for Family history of congenital anomalies is listed as V19.5.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | V19.5 |
| Long Description: | Family history of congenital anomalies |
| Short Description: | Fam hx-congen anomalies |
| Chapter: | Supplementary Classification Of Factors Influencing Health Status And Contact With Health Services |
| Block: | Persons With Potential Health Hazards Related To Personal And Family History (V10-V19) |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | Z82.79 - Family history of other congenital malformations, deformations and chromosomal abnormalities |
| ICD-9-CM Siblings (same level / similar specificity) of V19.5: | |
| V19.0 - Family history of blindness or visual loss | |
| V19.2 - Family history of deafness or hearing loss | |
| V19.3 - Family history of other ear disorders | |
| V19.4 - Family history of skin conditions | |
| V19.6 - Family history of allergic disorders | |
| V19.7 - Family history of consanguinity | |
| V19.8 - Family history of other condition | |