CONV. TYPE Unspecified pervasive developmental disorder YES NO Approx. F84.9 Pervasive developmental disorder, unspecified YES YES 307.
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1 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 Arom amin-acid metab NEC E70.30 Albinism, unspecified E70.5 Disorders of tryptophan metabolism E70.8 Other disorders of aromatic amino-acid metabolism Infantile Autism active state F84.0 Autistic disorder Autistic disorder, residual state F84.0 Autistic disorder 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 Unspecified pervasive developmental disorder F84.9 Pervasive developmental disorder, unspecified F50.8 Other eating disorders Other disorders of eating F98.29 Other feeding disorders of infancy and early childhood 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 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 Emotional dis child NEC F94.1 Reactive attachment disorder of childhood F98.8 Reactive attachment disorder of childhood 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 Attention Deficit/Hyperactivity Disorder-combined type F90.2 Attention-deficit hyperactivity disorder, combined type F90.9 Attention-deficit hyperactivity disorder, unspecified type Expressive language disorder Direct F80.1 Expressive language disorder Recp-expres language dis F80.2 Mixed receptive-expressive language disorder H93.25 Central auditory processing disorder Speech del d/t hear loss Direct F80.4 Speech and language development delay due to hearing loss Speech/language dis NEC F80.0 Phonological disorder F80.89 Other developmental disorders of speech and language Devel coordination dis F82 Specific developmental disorder of motor function Mixed development disorder F82 Specific developmental disorder of motor function Other specified delays in development F88 Other disorders of psychological development Development delay S F81.9 Developmental disorder of scholastic skills, unspecified F89 Unspecified disorder of psychological development Werdnig-Hoffmann disease Direct G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] Cerebral palsy S Direct G80.9 Cerebral palsy, unspecified Congenital diplegia Direct G80.1 Spastic diplegic cerebral palsy Congenital hemiplegia G80.2 Spastic hemiplegic cerebral palsy Congenital, quadriplegia Direct G80.0 Spastic quadriplegic cerebral palsy Infantile hemiplegia, G80.2 Spastic hemiplegic cerebral palsy Other specified infantile CP G80.8 Other cerebral palsy Infantile Spasms without Intractable Epilepsy Infantile Spasmswith intractable Epilepsy G G Epileptic spasms, not intractable, with status epilepticus Epileptic spasms, intractable, with status epilepticus G G Epileptic spasms, not intractable, without status epilepticus Epileptic spasms, intractable, without status epilepticus Cong hered musc dystrphy G71.2 Congenital myopathies ICD-9 --> 1 of 5
2 DESCRIPTION Myopathies NEC G72.89 Other specified myopathies Myopathy, unspecified G72.9 Myopathy, unspecified Retrolental fibroplasia H Retrolental fibroplasia, unspecified eye H Retinopathy of prematurity, stage 4, unspecified eye Retinoph prematr.stage 4 H Retinopathy of prematurity, stage 4, right eye H Retinopathy of prematurity, stage 4, left eye H Retinopathy of prematurity, stage 4, bilateral H Retinopathy of prematurity, stage 5, unspecified eye Retinoph prematr,stage 5 H Retinopathy of prematurity, stage 5, left eye H Retinopathy of prematurity, stage 5, right eye H Retinopathy of prematurity, stage 5, bilateral Hered retin dystrphy S Direct H35.50 Unspecified hereditary retinal dystrophy Blindness, both eyes H54.0 Blindness, both eyes Better eye: total vision impairment; lesser eye: total vision impairment H54.0 Blindness, both eyes H54.1 Blindness, one eye, low vision other eye Blindness, one eye, low vision other eye H54.10 Blindness, one eye, low vision other eye, unspecified eyes Low vision both eyes (moderate to severe) Better eye: moderate vision impairment; lesser eye: moderate vision impairment H54.2 Low vision, both eyes 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 Unspecified visual loss v41.0 Problems with sight H54.7 Unspecified visual loss Legal blindness, as defined in U.S.A H54.8 Legal blindness, as defined in USA H Coloboma of optic disc, unspecified eye Optic nerve coloboma (bilateral), acquired H Coloboma of optic disc, right eye H Coloboma of optic disc, left eye H Coloboma of optic disc, bilateral Visual deprivation nystagmus Direct H55.03 Visual deprivation nystagmus Congenital nystagmus Direct H55.01 Congenital nystagmus Conductive Hearing Loss - S Conductive hearing loss, external ear Conductive hearing loss, tympanic membrane Conductive hearing loss, middle ear H90.2 Conductive hearing loss, unspecified Conductive hearing loss of combined types Conductive hearing loss, inner ear 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 Conductive hearing loss, bilateral H90.0 Conductive hearing loss, bilateral Unspecified sensorineural hearing loss H90.5 Unspecified sensorineural hearing loss Sensory hearing loss, bilateral Neural hearing loss, bilateral H90.3 Sensorineural hearing loss, bilateral Neural hearing loss, unilateral Central hearing loss H90.5 Unspecified sensorineural hearing loss Sensorineural hearing loss, unilateral Sensorineural hearing loss, asymmetrical H90.5 Unspecified sensorineural hearing loss Sensory hearing loss, unilateral Sensorineural hearing loss, bilateral H90.3 Sensorineural hearing loss, bilateral ICD-9 --> 2 of 5
3 DESCRIPTION Mixed Conductive and Sensorineural Hearing Loss Direct H90.8 Mixed conductive and sensorineural hearing loss, unspecified 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 Mixed hearing loss, bilateral Direct H90.6 Mixed conductive and sensorineural hearing loss, bilateral Late effects of cerebrovascular disease, speech and language deficit, unspecified I Other speech and language deficits following unspecified cerebrovascular disease Torticollis, unspecified Direct M43.6 Torticollis Other specific muscle disorders M62.3 Immobility syndrome (paraplegic) M62.89 Other specified disorders of muscle Q05.4 Unspecified spina bifida with hydrocephalus 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 Muscle weakness (generalized) Direct M62.81 Muscle weakness (generalized) Unspecified disorder of muscle, ligament, and fascia M62.9 Disorder of muscle, unspecified Spin bif w hydrceph-cerv Direct Q05.0 Cervical spina bifida with hydrocephalus Spin bif w hydrceph-dors Direct Q05.1 Thoracic spina bifida with hydrocephalus Spin bif w hydrceph-lumb Q05.2 Lumbar spina bifida with hydrocephalus Spina Bifida w/o hydrocephalus (unspecified region) Q05.8 Sacral spina bifida without hydrocephalus Spina bifida-cerv Direct Q05.5 Cervical spina bifida without hydrocephalus Spina bifida-dorsal Direct Q05.6 Thoracic spina bifida without hydrocephalus Spina bifida-lumbar Direct Q05.7 Lumbar spina bifida without hydrocephalus Q01.9 Encephalocele, unspecified Q01.0 Frontal encephalocele Encephalocele Q01.1 Nasofrontal encephalocele Q01.2 Occipital encephalocele Q01.8 Encephalocele of other sites Q05.3 Sacral spina bifida with hydrocephalus Spina Bifida w/o hydrocephalus (unspecified region) Q05.8 Spina bifida without mention of hydrocephalus, unspecified region Microcephalus Direct Q02 Microcephaly Q04.1 Arhinencephaly 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 Congenital hydrocephalus Q03.1 Atresia of foramina of Magendie and Luschka Q03.8 Other congenital hydrocephalus Q03.9 Congenital hydrocephalus, unspecified Q04.5 Megalencephaly Brain anomaly NEC Q04.6 Congenital cerebral cysts Q04.8 Other specified congenital malformations of brain Aniridia Direct Q13.1 Absence of iris Optic nerve coloboma (bilateral), congenital Q14.2 Congenital malformation of optic disc Unspecified anomalies of the ear with hearing impairment Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified Cong absence ext ear Direct Q16.0 Congenital absence of (ear) auricle Ex ear anm NEC-impr hear Q16.1 Congenital absence, atresia and stricture of auditory canal (external) Middle ear anomaly NEC Direct Q16.4 Other congenital malformations of middle ear Anomalies of ear ossicles Direct Q16.3 Congenital malformation of ear ossicles Anomalies of inner ear Direct Q16.5 Congenital malformation of inner ear Other anomalies of ear causing impairment of hearing Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified Q35.9 Cleft palate, unspecified Cleft Palate Q35.3 Cleft soft palate Q35.5 Cleft hard palate with cleft soft palate Unilat cleft palate-comp Q35.9 Cleft palate, unspecified Unilat cleft palate-inc Q35.7 Cleft uvula Q35.9 Cleft palate, unspecified Bilat cleft palate-compl Q35.9 Cleft palate, unspecified Bilat cleft palate-inc Q35.9 Cleft palate, unspecified ICD-9 --> 3 of 5
4 DESCRIPTION Cleft lip S Q36.9 Cleft lip, unilateral Cleft lip, unilateral, complete Q36.9 Cleft lip, unilateral Bilat cleft lip-complete Q36.0 Cleft lip, bilateral Bilat cleft lip-incompl Q36.0 Cleft lip, bilateral Cleft palate & lip S Q37.9 Unspecified cleft palate with unilateral cleft lip Other combinations of cleft palate with cleft lip Q37.9 Unspecified cleft palate with unilateral cleft lip Congenital torticollis Direct Q68.0 Congenital deformity of sternocleidomastoid muscle Reduc deform up limb S Q Other reduction defects of unspecified upper limb Q71.90 Unspecified reduction defect of unspecified upper limb Reduction deform leg S Q Other reduction defects of unspecified lower limb Q73.0 Congenital absence of unspecified limb(s) Reduct deform limb S Q73.1 Phocomelia, unspecified limb(s) Q73.8 Other reduction defects of unspecified limb(s) Congen limb anomaly NEC Direct Q74.8 Other specified congenital malformations of limb(s) Q71.63 Lobster-claw hand, bilateral Lobster Claw (Hand) Q71.61 Lobster-claw right hand Q71.62 Lobster-claw left hand Q90.9 Down syndrome, unspecified 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 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) Edwards syndrome Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction) Q91.2 Trisomy 18, translocation Q91.3 Trisomy 18, unspecified Angelman's Syndrome (syndromes affecting multiple systems) Direct Q89.7 Multiple congenital malformations, not elsewhere classified Prader-Willi Syndrome Q87.1 Congenital malformation syndromes predominantly associated with short stature 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 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 Fetal Alcohol Syndrome Q86.0 Fetal alcohol syndrome (dysmorphic) P04.3 Newborn (suspected to be) affected by maternal use of alcohol Extreme Prematurity Less than 500 grams P07.01 Extremely low birth weight newborn, less than 500 grams Extreme Prematurity grams P07.02 Extremely low birth weight newborn, grams Extreme Prematurity grams P07.03 Extremely low birth weight newborn, grams Extreme immatur wts P07.00 Extremely low birth weight newborn, unspecified weight P07.10 Other low birth weight newborn, unspecified weight NB intraven hem,grade iv Direct P52.22 Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn Periventricular leukomalacia P91.2 Neonatal cerebral leukomalacia NB kernicterus P57.8 Other specified kernicterus P57.9 Kernicterus, unspecified R27.0 Ataxia, unspecified Lack of coordination R27.8 Other lack of coordination R27.9 Unspecified lack of coordination ICD-9 --> 4 of 5
5 Nerve/musculskel sym NEC DESCRIPTION R Other symptoms and signs involving the nervous system R 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 Lack norm physio dev S R62.50 Unspecified lack of expected normal physiological development in childhood Failure to thrive-child Direct R62.51 Failure to thrive (child) Delayed milestones Direct R62.0 Delayed milestone in childhood R47.02 Dysphasia Speech disturbance NEC R47.81 Slurred speech R47.89 Other speech disturbances R48.1 Agnosia Symbolic dysfunction NEC R48.2 Apraxia R48.8 Other symbolic dysfunctions 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 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
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