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Appendix 1: ICD-9 and ICD-10 developmental disabilities and related codes ADDIN CSL_CITATION {"citationItems":[{"id":"ITEM-1","itemData":{"ISBN":"9781926850450","editor":[{"dropping-particle":"","family":"Lunsky","given":"Yona","non-dropping-particle":"","parse-names":false,"suffix":""},{"dropping-particle":"","family":"Klein-Geltink","given":"Julia E.","non-dropping-particle":"","parse-names":false,"suffix":""},{"dropping-particle":"","family":"Yates","given":"Erika A.","non-dropping-particle":"","parse-names":false,"suffix":""}],"id":"ITEM-1","issue":"December","issued":{"date-parts":[["2013"]]},"publisher":"Institute for Clinical Evaluative Sciences and Centre for Addiction and Mental Health","publisher-place":"Toronto, ON","title":"Atlas on the Primary Care of Adults with Develop?mental Disabilities in Ontario","type":"book"},"uris":[""]}],"mendeley":{"formattedCitation":"(1)","plainTextFormattedCitation":"(1)"},"properties":{"noteIndex":0},"schema":""}(1)CodeLabelICD-9299-299.99Pervasive development disorders (e.g., autism)317–317.99Mental retardation318–318.99Mental retardation319–319.99Mental retardation758.0–758.39Chromosomal anomalies for which a developmental disability is typically present 758.5Other conditions due to autosomal anomalies758.8, 758.89Other conditions due to chromosome anomalies (do not include 75881)758.9Conditions due to anomaly of unspecified chromosome759.5Tuberous sclerosis759.81Other and unspecified congenital anomalies: Prader-Willi syndrome759.821Other and unspecified congenital anomalies: de Lange syndrome (include only if 6 digits exist, i.e., do not include 759.82)759.827Other and unspecified congenital anomalies: Seckel syndrome (include only if 6 digits exist)759.828Other and unspecified congenital anomalies: Smith-Lemli-Opitz syndrome (include only if 6 digits exist)759.83Other and unspecified congenital anomalies: Fragile X syndrome759.874Other and unspecified congenital anomalies: Beckwith-Wiedemann syndrome (include only if 6 digits exist)759.875Other and unspecified congenital anomalies: Zellweger syndrome (include only if 6 digits exist)759.89Other and unspecified congenital anomalies: other (e.g., Menkes disease, Laurence-Moon-Biedl syndrome, Rubinstein-Taybi syndrome)760.71Fetal alcohol syndrome760.77Fetal hydantoin syndromeICD-10F700Mild mental retardation with the statement of no, or minimal, impairment of behaviourF701Mild mental retardation, significant impairment of behaviour requiring attention or treatmentF708Mild mental retardation, other impairments of behaviourF709Mild mental retardation without mention of impairment of behaviourF710Moderate mental retardation with the statement of no, or minimal, impairment of behaviourF711Moderate mental retardation, significant impairment of behaviour requiring attention or treatmentF718Moderate mental retardation, other impairments of behaviourF719Moderate mental retardation without mention of impairment of behaviourF720Severe mental retardation with the statement of no, or minimal, impairment of behaviourF721Severe mental retardation, significant impairment of behaviour requiring attention or treatmentF728Severe mental retardation, other impairments of behaviourF729Severe mental retardation without mention of impairment of behaviourF730Profound mental retardation with the statement of no, or minimal, impairment of behaviourF731Profound mental retardation, significant impairment of behaviour requiring attention or treatmentF738Profound mental retardation, other impairments of behaviourF739Profound mental retardation without mention of impairment of behaviourF780Other mental retardation with the statement of no, or minimal, impairment of behaviourF781Other mental retardation, significant impairment of behaviour requiring attention or treatmentF788Other mental retardation, other impairments of behaviourF789Other mental retardation without mention of impairment of behaviourF79.0Unspecified mental retardation with the statement of no, or minimal, impairment of behaviourF791Unspecified mental retardation, significant impairment of behaviour requiring attention or treatmentF798Unspecified mental retardation, other impairments of behaviourF799Unspecified mental retardation without mention of impairment of behaviourF840Childhood autismF841Atypical autismF843Other childhood disintegrative disorderF844Overactive disorder associated with mental retardation and stereotyped movementsF845Asperger's syndromeF848Other pervasive developmental disordersF849Pervasive developmental disorder, unspecifiedQ851Tuberous sclerosisQ860Fetal alcohol syndromeQ861Fetal hydantoin syndromeQ871Aarskog, Prader-Willi, de Lange, Seckel, etc. Q8723Rubinstein-Taybi syndrome (include only if all 5 digits)Q8731Sotos syndrome (include only if all 5 digits)Q878OtherQ900–Q939 except Q926All Down syndrome types, cri du chat, etc., except extra marker chromosomesQ971Female with more than three X chromosomesQ992Fragile XQ998Other specified chromosome abnormalitiesDSM-IV299-299.80Pervasive developmental disorders317–317.99Mental retardation ................
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