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F01.50 Vascular dementia without behavioral disturbance |
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F01.51 Vascular dementia with behavioral disturbance |
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F02.80 Dementia in other diseases classified elsewhere without behavioral disturbance |
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F02.81 Dementia in other diseases classified elsewhere with behavioral disturbance |
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F03.90 Unspecified dementia without behavioral disturbance |
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F03.91 Unspecified dementia with behavioral disturbance |
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F06.0 Psychotic disorder with hallucinations due to known physiological condition |
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F06.1 Catatonic disorder due to known physiological condition |
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F06.2 Psychotic disorder with delusions due to known physiological condition |
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F06.30 Mood disorder due to known physiological condition, unspecified |
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F06.31 Mood disorder due to known physiological condition with depressive features |
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F06.32 Mood disorder due to known physiological condition with major depressive-like episode |
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F06.33 Mood disorder due to known physiological condition with manic features |
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F06.34 Mood disorder due to known physiological condition with mixed features |
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F06.4 Anxiety disorder due to known physiological condition |
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F06.8 Other specified mental disorders due to known physiological condition |
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F07.0 Personality change due to known physiological condition |
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F07.9 Unspecified personality and behavioral disorder due to known physiological condition |
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F63.3 Trichotillomania |
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F84.0 Autistic disorder |
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F84.3 Other childhood disintegrative disorder |
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Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction) |
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Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction) |
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Q90.2 Trisomy 21, translocation |
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Q90.9 Down syndrome, unspecified |
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Q91.0 Trisomy 18, nonmosaicism (meiotic nondisjunction) |
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Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction) |
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Q91.2 Trisomy 18, translocation |
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Q91.3 Trisomy 18, unspecified |
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Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction) |
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Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction) |
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Q91.6 Trisomy 13, translocation |
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Q91.7 Trisomy 13, unspecified |
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Q93.3 Deletion of short arm of chromosome 4 |
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Q93.4 Deletion of short arm of chromosome 5 |
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Q93.5 Other deletions of part of a chromosome |
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Q93.7 Deletions with other complex rearrangements |
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Q93.81 Velo-cardio-facial syndrome |
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Q93.88 Other microdeletions |
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Q93.89 Other deletions from the autosomes |
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Q93.9 Deletion from autosomes, unspecified |
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Q99.2 Fragile X chromosome |
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R40.4 Transient alteration of awareness |
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R41.81 Age-related cognitive decline |
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R41.841 Cognitive communication deficit |
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R41.843 Psychomotor deficit |
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R41.844 Frontal lobe and executive function deficit |
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R41.89 Other symptoms and signs involving cognitive functions and awareness |
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R45.1 Restlessness and agitation |
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R45.81 Low self-esteem |
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R45.82 Worries |
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