V19.3
ICD-9-CMThis code indicates a patient's family history of ear conditions that are not specifically categorized elsewhere. It signifies a genetic predisposition or familial pattern of ear diseases, excluding common conditions like otitis media or hearing loss, which have their own specific family history codes.
Use this code when a patient reports a family history of an ear disorder that doesn't fit into more specific family history categories (e.g., family history of Meniere's disease, otosclerosis, or other rare congenital ear anomalies). It is typically used as a secondary diagnosis to provide additional information about the patient's risk factors.
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Code History