Q16.5 – Congenital malformation of inner ear
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Applicable To
Congenital anomaly of membranous labyrinth
Congenital anomaly of organ of Corti
GEM Conversion to ICD-9 CM
Fs: 00000
–
Anomalies of inner ear
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Absence
(of) (organ or part) (complete or partial)
organ
Agenesis
organ
Anomaly, anomalous
(congenital) (unspecified type)
Q89.9
Aplasia
See also Agenesis
labyrinth, membranous
(congenital)
Q16.5
ear
(acquired)
See also Disorder, pinna, deformity
congenital
(external)
Q17.9
organ of Corti
(congenital)
Q16.5
Degeneration, degenerative
membranous labyrinth, congenital
(causing impairment of hearing)
Q16.5
saccule, congenital
(causing impairment of hearing)
Q16.5
Dilatation
Distortion
(s) (congenital)
organ
Enlargement, enlarged
See also Hypertrophy
Malformation
(congenital)
See also Anomaly
Mondini's malformation
(cochlea)
Q16.5
Sibling Codes
Parent Sibling Codes
View in Tabular
Code | Title |
---|---|
Q00-Q99 | Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) |
Q10-Q18 | Congenital malformations of eye, ear, face and neck (Q10-Q18) |
Q16 | Congenital malformations of ear causing impairment of hearing |
Q16.5 |
Congenital malformation of inner ear
Applicable to
Congenital anomaly of membranous labyrinth
Congenital anomaly of organ of Corti
|