Billable/Specific ICD-10-CM Codes - Page 47
There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.
- F80.9 - Developmental disorder of speech and language, unspecified
- F81.0 - Specific reading disorder
- F81.2 - Mathematics disorder
- F81.81 - Disorder of written expression
- F81.89 - Other developmental disorders of scholastic skills
- F81.9 - Developmental disorder of scholastic skills, unspecified
- F84.0 - Autistic disorder
- F84.2 - Rett's syndrome
- F84.3 - Other childhood disintegrative disorder
- F84.5 - Asperger's syndrome
- F84.8 - Other pervasive developmental disorders
- F84.9 - Pervasive developmental disorder, unspecified
- F90.0 - Attention-deficit hyperactivity disorder, predominantly inattentive type
- F90.1 - Attention-deficit hyperactivity disorder, predominantly hyperactive type
- F90.2 - Attention-deficit hyperactivity disorder, combined type
- F90.8 - Attention-deficit hyperactivity disorder, other type
- F90.9 - Attention-deficit hyperactivity disorder, unspecified type
- F91.0 - Conduct disorder confined to family context
- F91.1 - Conduct disorder, childhood-onset type
- F91.2 - Conduct disorder, adolescent-onset type
- F91.3 - Oppositional defiant disorder
- F91.8 - Other conduct disorders
- F91.9 - Conduct disorder, unspecified
- F93.0 - Separation anxiety disorder of childhood
- F93.8 - Other childhood emotional disorders
- F93.9 - Childhood emotional disorder, unspecified
- F94.0 - Selective mutism
- F94.1 - Reactive attachment disorder of childhood
- F94.2 - Disinhibited attachment disorder of childhood
- F94.8 - Other childhood disorders of social functioning
- F94.9 - Childhood disorder of social functioning, unspecified
- F95.0 - Transient tic disorder
- F95.1 - Chronic motor or vocal tic disorder
- F95.2 - Tourette's disorder
- F95.8 - Other tic disorders
- F95.9 - Tic disorder, unspecified
- F98.0 - Enuresis not due to a substance or known physiological condition
- F98.1 - Encopresis not due to a substance or known physiological condition
- F98.21 - Rumination disorder of infancy and childhood
- F98.29 - Other feeding disorders of infancy and early childhood
- F98.3 - Pica of infancy and childhood
- F98.4 - Stereotyped movement disorders
- F98.5 - Adult onset fluency disorder
- F98.8 - Other specified behavioral and emotional disorders with onset usually occurring in childhood and adolescence
- F98.9 - Unspecified behavioral and emotional disorders with onset usually occurring in childhood and adolescence
- G00.0 - Hemophilus meningitis
- G00.1 - Pneumococcal meningitis
- G00.2 - Streptococcal meningitis
- G00.3 - Staphylococcal meningitis
- G00.8 - Other bacterial meningitis
- G00.9 - Bacterial meningitis, unspecified
- G03.0 - Nonpyogenic meningitis
- G03.1 - Chronic meningitis
- G03.2 - Benign recurrent meningitis [Mollaret]
- G03.8 - Meningitis due to other specified causes
- G03.9 - Meningitis, unspecified
- G04.00 - Acute disseminated encephalitis and encephalomyelitis, unspecified
- G04.01 - Postinfectious acute disseminated encephalitis and encephalomyelitis (postinfectious ADEM)
- G04.02 - Postimmunization acute disseminated encephalitis, myelitis and encephalomyelitis
- G04.1 - Tropical spastic paraplegia
- G04.2 - Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
- G04.30 - Acute necrotizing hemorrhagic encephalopathy, unspecified
- G04.31 - Postinfectious acute necrotizing hemorrhagic encephalopathy
- G04.32 - Postimmunization acute necrotizing hemorrhagic encephalopathy
- G04.39 - Other acute necrotizing hemorrhagic encephalopathy
- G04.81 - Other encephalitis and encephalomyelitis
- G04.82 - Acute flaccid myelitis
- G04.89 - Other myelitis
- G04.90 - Encephalitis and encephalomyelitis, unspecified
- G04.91 - Myelitis, unspecified
- G05.3 - Encephalitis and encephalomyelitis in diseases classified elsewhere
- G05.4 - Myelitis in diseases classified elsewhere
- G06.0 - Intracranial abscess and granuloma
- G06.1 - Intraspinal abscess and granuloma
- G06.2 - Extradural and subdural abscess, unspecified
- G11.0 - Congenital nonprogressive ataxia
- G11.10 - Early-onset cerebellar ataxia, unspecified
- G11.11 - Friedreich ataxia
- G11.19 - Other early-onset cerebellar ataxia
- G11.2 - Late-onset cerebellar ataxia
- G11.3 - Cerebellar ataxia with defective DNA repair
- G11.4 - Hereditary spastic paraplegia
- G11.5 - Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6 - Leukodystrophy with vanishing white matter disease
- G11.8 - Other hereditary ataxias
- G11.9 - Hereditary ataxia, unspecified
- G12.0 - Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
- G12.1 - Other inherited spinal muscular atrophy
- G12.20 - Motor neuron disease, unspecified
- G12.21 - Amyotrophic lateral sclerosis
- G12.22 - Progressive bulbar palsy
- G12.23 - Primary lateral sclerosis
- G12.24 - Familial motor neuron disease
- G12.25 - Progressive spinal muscle atrophy
- G12.29 - Other motor neuron disease
- G12.8 - Other spinal muscular atrophies and related syndromes
- G12.9 - Spinal muscular atrophy, unspecified
- G13.0 - Paraneoplastic neuromyopathy and neuropathy
- G13.1 - Other systemic atrophy primarily affecting central nervous system in neoplastic disease
- G13.2 - Systemic atrophy primarily affecting the central nervous system in myxedema