2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Symptoms, Signs, And Ill-Defined Conditions 780-799 > Symptoms 780-789 > Symptoms Concerning Nutrition Metabolism And Development 783.* > 2008 ICD-9-CM Diagnosis 783.9
Other symptoms concerning nutrition metabolism and development On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.
The 2009 version of ICD-9-CM 783.9 can be accessed here. - 783.9 is a specific code that can be used to specify a diagnosis
- 783.9 contains 9 index entries
- View the ICD-9-CM Volume 1 783.* hierarchy
783.9 also known as: 783.9 excludes: - abnormal basal metabolic rate (794.7)
- dehydration (276.51)
- other disorders of fluid, electrolyte, and acid-base balance (276.0-276.9)
Index entries containing 783.9:- Abnormal, abnormality, abnormalities - see also Anomaly
- increase in
- development
783.9
- metabolism (see also condition)
783.9
Dystrophy, dystrophia 783.9- adiposogenital 253.8
- asphyxiating thoracic 756.4
- Becker's type 359.22
- brevicollis 756.16
- Bruch's membrane 362.77
- cervical (sympathetic) NEC 337.0
- chondro-osseus with punctate epiphyseal dysplasia 756.59
- choroid (hereditary) 363.50
- central (areolar) (partial) 363.53
- circinate 363.53
- circumpapillary (partial) 363.51
- diffuse
- generalized
- gyrate
- helicoid 363.52
- peripapillary - see Dystrophy, choroid, circumpapillary
- serpiginous 363.54
- cornea (hereditary) 371.50
- dermatochondrocorneal 371.50
- Duchenne's 359.1
- due to malnutrition 263.9
- Erb's 359.1
- familial
- foveal 362.77
- Fuchs', cornea 371.57
- Gowers' muscular 359.1
- hair 704.2
- hereditary, progressive muscular 359.1
- hypogenital, with diabetic tendency 759.81
- Landouzy-Déjérine 359.1
- Leyden-Möbius 359.1
- mesodermalis congenita 759.82
- muscular 359.1
- myocardium, myocardial (see also Degeneration, myocardial) 429.1
- myotonic 359.21
- myotonica 359.21
- nail 703.8
- neurovascular (traumatic) (see also Neuropathy, peripheral, autonomic) 337.9
- nutritional 263.9
- ocular 359.1
- oculocerebrorenal 270.8
- oculopharyngeal 359.1
- ovarian 620.8
- papillary (and pigmentary) 701.1
- pelvicrural atrophic 359.1
- pigmentary (see also Acanthosis) 701.2
- pituitary (gland) 253.8
- polyglandular 258.8
- posttraumatic sympathetic - see Dystrophy, symphatic
- progressive ophthalmoplegic 359.1
- retina, retinal (hereditary) 362.70
- Salzmann's nodular 371.46
- scapuloperoneal 359.1
- skin NEC 709.9
- sympathetic (posttraumatic) (reflex) 337.20
- tapetoretinal NEC 362.74
- thoracic asphyxiating 756.4
- unguium 703.8
- vitreoretinal (primary) 362.73
- vulva 624.09
Hypometabolism 783.9 Increase, increased- abnormal, in development
783.9
Large- stature
783.9
Symptoms, specified (general) NEC 780.99- development NEC
783.9
- metabolism NEC
783.9
- nutrition, metabolism, and development NEC
783.9
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