DRG 884 - List of Diagnostic Related Groups (MS-DRG v38.1)
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DRG 884 Organic disturbances and intellectual disability
- F01.50 Vascular dementia without behavioral disturbance
- F01.51 Vascular dementia with behavioral disturbance
- F02.80 Dementia in oth diseases classd elswhr w/o behavrl disturb
- F02.81 Dementia in oth diseases classd elswhr w behavioral disturb
- F03.90 Unspecified dementia without behavioral disturbance
- F03.91 Unspecified dementia with behavioral disturbance
- F04 Amnestic disorder due to known physiological condition
- F06.0 Psychotic disorder w hallucin due to known physiol condition
- F06.1 Catatonic disorder due to known physiological condition
- F06.2 Psychotic disorder w delusions due to known physiol cond
- F06.30 Mood disorder due to known physiological condition, unsp
- F06.31 Mood disorder due to known physiol cond w depressv features
- F06.32 Mood disord d/t physiol cond w major depressive-like epsd
- F06.33 Mood disorder due to known physiol cond w manic features
- F06.34 Mood disorder due to known physiol cond w mixed features
- F06.4 Anxiety disorder due to known physiological condition
- F06.8 Oth mental disorders due to known physiological condition
- F07.0 Personality change due to known physiological condition
- F07.9 Unsp personality & behavrl disord due to known physiol cond
- F09 Unsp mental disorder due to known physiological condition
- F54 Psych & behavrl factors assoc w disord or dis classd elswhr
- F63.3 Trichotillomania
- F70 Mild intellectual disabilities
- F71 Moderate intellectual disabilities
- F72 Severe intellectual disabilities
- F73 Profound intellectual disabilities
- F78 Other intellectual disabilities
- F79 Unspecified intellectual disabilities
- F84.0 Autistic disorder
- F84.3 Other childhood disintegrative disorder
- Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction)
- Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
- Q90.2 Trisomy 21, translocation
- Q90.9 Down syndrome, unspecified
- Q91.0 Trisomy 18, nonmosaicism (meiotic nondisjunction)
- Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)
- Q91.2 Trisomy 18, translocation
- Q91.3 Trisomy 18, unspecified
- Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction)
- Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)
- Q91.6 Trisomy 13, translocation
- Q91.7 Trisomy 13, unspecified
- Q93.3 Deletion of short arm of chromosome 4
- Q93.4 Deletion of short arm of chromosome 5
- Q93.51 Angelman syndrome
- Q93.59 Other deletions of part of a chromosome
- Q93.7 Deletions with other complex rearrangements
- Q93.81 Velo-cardio-facial syndrome
- Q93.82 Williams syndrome
- Q93.88 Other microdeletions
- Q93.89 Other deletions from the autosomes
- Q93.9 Deletion from autosomes, unspecified
- Q99.2 Fragile X chromosome
- R40.4 Transient alteration of awareness
- R41.81 Age-related cognitive decline
- R41.841 Cognitive communication deficit
- R41.843 Psychomotor deficit
- R41.844 Frontal lobe and executive function deficit
- R41.89 Oth symptoms and signs w cognitive functions and awareness
- R45.1 Restlessness and agitation
- R45.81 Low self-esteem
- R45.82 Worries
- R54 Age-related physical debility