H47.22

Hereditary optic atrophy

Billable / specific

H47.22 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Note: Use an external cause code following the code for the eye condition, if applicable, to identify the cause of the eye condition

Not included here — may be reported together when both conditions exist.

certain conditions originating in the perinatal period (P04-P96) (from H47)
certain infectious and parasitic diseases (A00-B99) (from H47)
complications of pregnancy, childbirth and the puerperium (O00-O9A) (from H47)
congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from H47)
diabetes mellitus related eye conditions (E09.3-, E10.3-, E11.3-, E13.3-) (from H47)
endocrine, nutritional and metabolic diseases (E00-E88) (from H47)
injury (trauma) of eye and orbit (S05.-) (from H47)
injury, poisoning and certain other consequences of external causes (S00-T88) (from H47)
neoplasms (C00-D49) (from H47)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from H47)
syphilis related eye disorders (A50.01, A50.3-, A51.43, A52.71) (from H47)