to Conversion Table Billing Code: Billable ICD-9/ -CM code that can be used to indicate a diagnosis for reimbursement purpose Eligibility Code: ICD-9/ associated with diagnosed conditions with a high probability of and related to EIP eligibility Conversion (Conv.) Type: : Require clinical interpretation in order to determine the most appropriate conversion code(s) for your specific coding situation. Direct: An exact conversion from ICD-9 to ICD-9 DESCRIPTION E70.21 Tyrosinemia E70.29 Other disorders of tyrosine metabolism 270.2 Arom amin-acid metab NEC E70.30 Albinism, unspecified E70.5 Disorders of tryptophan metabolism E70.8 Other disorders of aromatic amino-acid metabolism 299.00 Infantile Autism active state F84.0 Autistic disorder 299.01 Autistic disorder, residual state F84.0 Autistic disorder 299.80 299.81 Pervasive Developmental Disorder (PDD) Other specified pervasive developmental disorders, residual state F84.5 F84.5 Asperger's syndrome Asperger's syndrome F84.8 F84.8 Other pervasive developmental disorders Other pervasive developmental disorders 299.9 Unspecified pervasive developmental disorder F84.9 Pervasive developmental disorder, unspecified 307.59 F50.8 Other eating disorders Other disorders of eating F98.29 Other feeding disorders of infancy and early childhood 309.81 Prolonged Post Traumatic Stress Disorder F43.10 Post-traumatic stress disorder, unspecified F43.12 Post-traumatic stress disorder, chronic F93.9 Childhood emotional disorder, unspecified F94.8 Other childhood disorders of social functioning 313.9 Emotional dis child S Unspecified behavioral and emotional disorders with onset usually occurring in F98.9 childhood and adolescence F93.8 Other childhood emotional disorders 313.89 Emotional dis child NEC F94.1 Reactive attachment disorder of childhood F98.8 Reactive attachment disorder of childhood 314.00 Prolonged Attention Deficit Disorder w/o Hyperactivity F90.0 Attention-deficit hyperactivity disorder, predominantly inattentive type F90.9 Attention-deficit hyperactivity disorder, unspecified type F90.1 Attention-deficit hyperactivity disorder, predominantly hyperactive type 314.01 Attention Deficit/Hyperactivity Disorder-combined type F90.2 Attention-deficit hyperactivity disorder, combined type F90.9 Attention-deficit hyperactivity disorder, unspecified type 315.31 Expressive language disorder Direct F80.1 Expressive language disorder 315.32 Recp-expres language dis F80.2 Mixed receptive-expressive language disorder H93.25 Central auditory processing disorder 315.34 Speech del d/t hear loss Direct F80.4 Speech and language development delay due to hearing loss 315.39 Speech/language dis NEC F80.0 Phonological disorder F80.89 Other developmental disorders of speech and language 315.4 Devel coordination dis F82 Specific developmental disorder of motor function 315.5 Mixed development disorder F82 Specific developmental disorder of motor function 315.8 Other specified delays in development F88 Other disorders of psychological development 315.9 Development delay S F81.9 Developmental disorder of scholastic skills, unspecified F89 Unspecified disorder of psychological development 335.0 Werdnig-Hoffmann disease Direct G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] 343.9 Cerebral palsy S Direct G80.9 Cerebral palsy, unspecified 343.0 Congenital diplegia Direct G80.1 Spastic diplegic cerebral palsy 343.1 Congenital hemiplegia G80.2 Spastic hemiplegic cerebral palsy 343.2 Congenital, quadriplegia Direct G80.0 Spastic quadriplegic cerebral palsy 343.4 Infantile hemiplegia, G80.2 Spastic hemiplegic cerebral palsy 343.8 Other specified infantile CP G80.8 Other cerebral palsy 345.60 345.61 Infantile Spasms without Intractable Epilepsy Infantile Spasmswith intractable Epilepsy G40.821 G40.823 Epileptic spasms, not intractable, with status epilepticus Epileptic spasms, intractable, with status epilepticus G40.821 G40.824 Epileptic spasms, not intractable, without status epilepticus Epileptic spasms, intractable, without status epilepticus 359.0 Cong hered musc dystrphy G71.2 Congenital myopathies ICD-9 --> 1 of 5
DESCRIPTION 359.89 Myopathies NEC G72.89 Other specified myopathies 359.9 Myopathy, unspecified G72.9 Myopathy, unspecified 362.21 Retrolental fibroplasia H35.179 Retrolental fibroplasia, unspecified eye H35.159 Retinopathy of prematurity, stage 4, unspecified eye 362.26 Retinoph prematr.stage 4 H35.151 Retinopathy of prematurity, stage 4, right eye H35.152 Retinopathy of prematurity, stage 4, left eye H35.153 Retinopathy of prematurity, stage 4, bilateral H35.169 Retinopathy of prematurity, stage 5, unspecified eye 362.27 Retinoph prematr,stage 5 H35.162 Retinopathy of prematurity, stage 5, left eye H35.161 Retinopathy of prematurity, stage 5, right eye H35.163 Retinopathy of prematurity, stage 5, bilateral 362.70 Hered retin dystrphy S Direct H35.50 Unspecified hereditary retinal dystrophy 369.00 Blindness, both eyes H54.0 Blindness, both eyes 369.01 Better eye: total vision impairment; lesser eye: total vision impairment H54.0 Blindness, both eyes H54.1 Blindness, one eye, low vision other eye 369.10 Blindness, one eye, low vision other eye H54.10 Blindness, one eye, low vision other eye, unspecified eyes 369.20 Low vision both eyes (moderate to severe) 369.25 Better eye: moderate vision impairment; lesser eye: moderate vision impairment H54.2 Low vision, both eyes 369.3 Unqualified visual loss, both eyes Direct H54.3 Unqualified visual loss, both eyes H54.4 Blindness, one eye H54.5 Low vision, one eye H54.6 Unqualified visual loss, one eye 369.9 Unspecified visual loss v41.0 Problems with sight H54.7 Unspecified visual loss 369.4 Legal blindness, as defined in U.S.A H54.8 Legal blindness, as defined in USA H47.319 Coloboma of optic disc, unspecified eye 377.23 Optic nerve coloboma (bilateral), acquired H47.311 Coloboma of optic disc, right eye H47.312 Coloboma of optic disc, left eye H47.313 Coloboma of optic disc, bilateral 379.53 Visual deprivation nystagmus Direct H55.03 Visual deprivation nystagmus 379.51 Congenital nystagmus Direct H55.01 Congenital nystagmus 389.00 Conductive Hearing Loss - S 389.01 Conductive hearing loss, external ear 389.02 Conductive hearing loss, tympanic membrane 389.03 Conductive hearing loss, middle ear H90.2 Conductive hearing loss, unspecified 389.08 Conductive hearing loss of combined types 389.04 Conductive hearing loss, inner ear 389.05 Conductive hearing loss, inner ear H90.11 Conductive hearing loss, unilateral, right ear, with unrestricted hearing on the H90.12 Conductive hearing loss, unilateral, left ear, with unrestricted hearing on the 389.06 Conductive hearing loss, bilateral H90.0 Conductive hearing loss, bilateral 389.10 Unspecified sensorineural hearing loss H90.5 Unspecified sensorineural hearing loss 389.11 Sensory hearing loss, bilateral 389.12 Neural hearing loss, bilateral H90.3 Sensorineural hearing loss, bilateral 389.13 Neural hearing loss, unilateral 389.14 Central hearing loss H90.5 Unspecified sensorineural hearing loss 389.15 Sensorineural hearing loss, unilateral 389.16 Sensorineural hearing loss, asymmetrical H90.5 Unspecified sensorineural hearing loss 389.17 Sensory hearing loss, unilateral 389.18 Sensorineural hearing loss, bilateral H90.3 Sensorineural hearing loss, bilateral ICD-9 --> 2 of 5
DESCRIPTION 389.20 Mixed Conductive and Sensorineural Hearing Loss Direct H90.8 Mixed conductive and sensorineural hearing loss, unspecified 389.21 Mixed hearing loss, unilateral H90.71 Mixed conductive and sensorineural hearing loss, unilateral, right ear, with unrestricted hearing on the H90.72 Mixed conductive and sensorineural hearing loss, unilateral, left ear, with unrestricted hearing on the 389.22 Mixed hearing loss, bilateral Direct H90.6 Mixed conductive and sensorineural hearing loss, bilateral 438.1 Late effects of cerebrovascular disease, speech and language deficit, unspecified I69.928 Other speech and language deficits following unspecified cerebrovascular disease 723.5 Torticollis, unspecified Direct M43.6 Torticollis 728.3 Other specific muscle disorders M62.3 Immobility syndrome (paraplegic) M62.89 Other specified disorders of muscle Q05.4 Unspecified spina bifida with hydrocephalus 741.00 Spina Bifida with hydrocephalus (unspecified region) Q07.01 Arnold-Chiari syndrome with spina bifida Q07.02 Arnold-Chiari syndrome with hydrocephalus Q07.03 Arnold-Chiari syndrome with spina bifida and hydrocephalus 728.87 Muscle weakness (generalized) Direct M62.81 Muscle weakness (generalized) 728.9 Unspecified disorder of muscle, ligament, and fascia M62.9 Disorder of muscle, unspecified 741.01 Spin bif w hydrceph-cerv Direct Q05.0 Cervical spina bifida with hydrocephalus 741.02 Spin bif w hydrceph-dors Direct Q05.1 Thoracic spina bifida with hydrocephalus 741.03 Spin bif w hydrceph-lumb Q05.2 Lumbar spina bifida with hydrocephalus 741.90 Spina Bifida w/o hydrocephalus (unspecified region) Q05.8 Sacral spina bifida without hydrocephalus 741.91 Spina bifida-cerv Direct Q05.5 Cervical spina bifida without hydrocephalus 741.92 Spina bifida-dorsal Direct Q05.6 Thoracic spina bifida without hydrocephalus 741.93 Spina bifida-lumbar Direct Q05.7 Lumbar spina bifida without hydrocephalus Q01.9 Encephalocele, unspecified Q01.0 Frontal encephalocele 742.0 Encephalocele Q01.1 Nasofrontal encephalocele Q01.2 Occipital encephalocele Q01.8 Encephalocele of other sites Q05.3 Sacral spina bifida with hydrocephalus 741.90 Spina Bifida w/o hydrocephalus (unspecified region) Q05.8 Spina bifida without mention of hydrocephalus, unspecified region 742.1 Microcephalus Direct Q02 Microcephaly Q04.1 Arhinencephaly 742.2 Reduction deform, brain Q04.2 Holoprosencephaly Q04.3 Other reduction deformities of brain Q04.0 agenesis of corpus callosum Q03.0 Malformations of aqueduct of Sylvius 742.3 Congenital hydrocephalus Q03.1 Atresia of foramina of Magendie and Luschka Q03.8 Other congenital hydrocephalus Q03.9 Congenital hydrocephalus, unspecified Q04.5 Megalencephaly 742.4 Brain anomaly NEC Q04.6 Congenital cerebral cysts Q04.8 Other specified congenital malformations of brain 743.45 Aniridia Direct Q13.1 Absence of iris 743.57 Optic nerve coloboma (bilateral), congenital Q14.2 Congenital malformation of optic disc 744.00 Unspecified anomalies of the ear with hearing impairment Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified 744.01 Cong absence ext ear Direct Q16.0 Congenital absence of (ear) auricle 744.02 Ex ear anm NEC-impr hear Q16.1 Congenital absence, atresia and stricture of auditory canal (external) 744.03 Middle ear anomaly NEC Direct Q16.4 Other congenital malformations of middle ear 744.04 Anomalies of ear ossicles Direct Q16.3 Congenital malformation of ear ossicles 744.05 Anomalies of inner ear Direct Q16.5 Congenital malformation of inner ear 744.09 Other anomalies of ear causing impairment of hearing Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified Q35.9 Cleft palate, unspecified 749.00 Cleft Palate Q35.3 Cleft soft palate Q35.5 Cleft hard palate with cleft soft palate 749.01 Unilat cleft palate-comp Q35.9 Cleft palate, unspecified 749.02 Unilat cleft palate-inc Q35.7 Cleft uvula Q35.9 Cleft palate, unspecified 749.03 Bilat cleft palate-compl Q35.9 Cleft palate, unspecified 749.04 Bilat cleft palate-inc Q35.9 Cleft palate, unspecified ICD-9 --> 3 of 5
DESCRIPTION 749.10 Cleft lip S Q36.9 Cleft lip, unilateral 749.11 Cleft lip, unilateral, complete Q36.9 Cleft lip, unilateral 749.13 Bilat cleft lip-complete Q36.0 Cleft lip, bilateral 749.14 Bilat cleft lip-incompl Q36.0 Cleft lip, bilateral 749.20 Cleft palate & lip S Q37.9 Unspecified cleft palate with unilateral cleft lip 749.25 Other combinations of cleft palate with cleft lip Q37.9 Unspecified cleft palate with unilateral cleft lip 754.1 Congenital torticollis Direct Q68.0 Congenital deformity of sternocleidomastoid muscle 755.20 Reduc deform up limb S Q71.899 Other reduction defects of unspecified upper limb Q71.90 Unspecified reduction defect of unspecified upper limb 755.30 Reduction deform leg S Q72.899 Other reduction defects of unspecified lower limb Q73.0 Congenital absence of unspecified limb(s) 755.4 Reduct deform limb S Q73.1 Phocomelia, unspecified limb(s) Q73.8 Other reduction defects of unspecified limb(s) 755.8 Congen limb anomaly NEC Direct Q74.8 Other specified congenital malformations of limb(s) Q71.63 Lobster-claw hand, bilateral 755.58 Lobster Claw (Hand) Q71.61 Lobster-claw right hand Q71.62 Lobster-claw left hand Q90.9 Down syndrome, unspecified 758.0 Down syndrome Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction) Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction) Q90.2 Trisomy 21, translocation Q91.7 Trisomy 13, unspecified 758.1 Pataus syndrome Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction) Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction) Q91.6 Trisomy 13, translocation Q91.3 Trisomy 18, unspecified Q91.0 Trisomy 18, nonmosaicism (meiotic nondisjunction) 758.2 Edwards syndrome Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction) Q91.2 Trisomy 18, translocation Q91.3 Trisomy 18, unspecified 759.7 Angelman's Syndrome (syndromes affecting multiple systems) Direct Q89.7 Multiple congenital malformations, not elsewhere classified 759.81 Prader-Willi Syndrome Q87.1 Congenital malformation syndromes predominantly associated with short stature 759.83 Fragile X Syndrome Direct Q99.2 Fragile X chromosome E78.71 Barth syndrome E78.72 Smith-Lemli-Opitz syndrome Q87.2 Congenital malformation syndromes predominantly involving limbs Q87.3 Congenital malformation syndromes involving early overgrowth 759.89 CHARGE Association Q87.5 Other congenital malformation syndromes with other skeletal changes Q87.81 Alport syndrome Q87.89 Other specified congenital malformation syndromes, not elsewhere classified Q89.8 Other specified congenital malformations 760.71 Fetal Alcohol Syndrome Q86.0 Fetal alcohol syndrome (dysmorphic) P04.3 Newborn (suspected to be) affected by maternal use of alcohol 765.01 Extreme Prematurity Less than 500 grams P07.01 Extremely low birth weight newborn, less than 500 grams 765.02 Extreme Prematurity 500-749 grams P07.02 Extremely low birth weight newborn, 500-749 grams 765.03 Extreme Prematurity 750-999 grams P07.03 Extremely low birth weight newborn, 750-999 grams 765.00 Extreme immatur wts P07.00 Extremely low birth weight newborn, unspecified weight P07.10 Other low birth weight newborn, unspecified weight 772.14 NB intraven hem,grade iv Direct P52.22 Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn 779.7 Periventricular leukomalacia P91.2 Neonatal cerebral leukomalacia 774.7 NB kernicterus P57.8 Other specified kernicterus P57.9 Kernicterus, unspecified R27.0 Ataxia, unspecified 781.3 Lack of coordination R27.8 Other lack of coordination R27.9 Unspecified lack of coordination ICD-9 --> 4 of 5
781.99 Nerve/musculskel sym NEC DESCRIPTION R29.818 Other symptoms and signs involving the nervous system R29.898 Other symptoms and signs involving the musculoskeletal system R29.90 Unspecified symptoms and signs involving the nervous system R29.91 Unspecified symptoms and signs involving the musculoskeletal system 783.40 Lack norm physio dev S R62.50 Unspecified lack of expected normal physiological development in childhood 783.41 Failure to thrive-child Direct R62.51 Failure to thrive (child) 783.42 Delayed milestones Direct R62.0 Delayed milestone in childhood R47.02 Dysphasia 784.59 Speech disturbance NEC R47.81 Slurred speech R47.89 Other speech disturbances R48.1 Agnosia 784.69 Symbolic dysfunction NEC R48.2 Apraxia R48.8 Other symbolic dysfunctions 799.9 Unkn cause morb/mort NEC R69 Illness, unspecified R99 Ill-defined and unknown cause of mortality S14.109A Unspecified injury at unspecified level of cervical spinal cord, initial encounter 952.9 Spinal cord injury S S24.109A Unspecified injury at unspecified level of thoracic spinal cord, initial encounter S34.109A Unspecified injury to unspecified level of lumbar spinal cord, initial encounter S34.139A Unspecified injury to sacral spinal cord, initial encounter ICD-9 --> 5 of 5