2011 ICD-9-CM Diagnosis Code 783.9 : Other symptoms concerning nutrition metabolism and development

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2011 ICD-9-CM Diagnosis Code 783.9

Other symptoms concerning nutrition metabolism and development

Short description: Nutr/metab/devel sym NEC.
ICD-9-CM 783.9 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 783.9 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
You are viewing the 2011 version of ICD-9-CM 783.9.
More recent version(s) of ICD-9-CM 783.9: 2012 2013 2014 2015.

Convert to ICD-10-CM: 783.9 converts approximately to:

2015/16 ICD-10-CM R63.8 Other symptoms and signs concerning food and fluid intake

Approximate Synonyms

Abnl increase in body height
ABNL INCREASE IN BODY HEIGHT (finding)
Abnormal increase in body height
Abnormal metabolic state in diabetes mellitus
Abnormal sexual state and development
Abnormal weight
Adipsia
Altered appetite
Appetite problem
Body weight AND/OR growth problem
Carbohydrate craving
Childhood growth AND/OR development alteration
Decrease in appetite
Decreased body growth
Decreased metabolic requirement
Developmental delay in feeding
Dietary potassium - high
Difficulty eating
Disorder of stature
Disorders with tall stature
Excessive dietary caloric intake
Excessive dietary carbohydrate intake
Excessive dietary intake of calcium
Excessive dietary intake of fat
Excessive dietary intake of fiber
Excessive dietary intake of folate
Excessive dietary intake of iron
Excessive dietary intake of niacin
Excessive dietary intake of potassium
Excessive dietary intake of protein
Excessive dietary intake of riboflavin
Excessive dietary intake of thiamine
Excessive dietary intake of vitamin A
Excessive dietary intake of vitamin C
Excessive dietary intake of vitamin D
Excessive dietary intake of vitamin E
Excessive dietary intake of vitamin K
Excessive dietary intake of zinc
Excessive dietary mineral intake
Excessive dietary vitamin intake
Failure to lose weight
Failure to maintain weight
Folate deficiency anemia due to dietary causes
Hypometabolism
Inadequate dietary intake of vitamin D
Increased appetite
Increased body growth
Increased metabolic requirement
Infant formula for metabolic dysfunction
Nutritional disorder
Nutritionally compromised
On examination - endocrine, nutrition or metabolic
On examination - failure to thrive
On examination - height greater than 20% over average
On examination - lack of growth
On examination - underactive infant
On examination - weight 10-20% below ideal
On examination - weight greater than 20% below ideal
Patchy organ or tissue uptake
Post-pubertal
Pre-pubertal
Pubertal
Sequelae of nutritional disorders
Sexual nondevelopment
Slow weight gain
Tall for age
Tall stature
Thin build
Weight decreased
Weight increased

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)

Applies To

Hypometabolism

ICD-9-CM Volume 2 Index entries containing back-references to 783.9:

Abnormal, abnormality, abnormalities - see also Anomaly
- increase in
  - appetite 783.6
  - 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 337.09
- chondro-osseus with punctate epiphyseal dysplasia 756.59
- choroid (hereditary) 363.50
  - central (areolar) (partial) 363.53
    - total (gyrate) 363.54
  - circinate 363.53
  - circumpapillary (partial) 363.51
    - total 363.52
  - diffuse
    - partial 363.56
    - total 363.57
  - generalized
    - partial 363.56
    - total 363.57
  - gyrate
    - central 363.54
    - generalized 363.57
  - helicoid 363.52
  - peripapillary - see Dystrophy, choroid, circumpapillary
  - serpiginous 363.54
- cornea (hereditary) 371.50
  - anterior NEC 371.52
  - Cogan's 371.52
  - combined 371.57
  - crystalline 371.56
  - endothelial (Fuchs') 371.57
  - epithelial 371.50
    - juvenile 371.51
    - microscopic cystic 371.52
  - granular 371.53
  - lattice 371.54
  - macular 371.55
  - marginal (Terrien's) 371.48
  - meesman's 371.51
  - microscopic cystic (epithelial) 371.52
  - nodular, Salzmann's 371.46
  - polymorphous 371.58
  - posterior NEC 371.58
  - ring-like 371.52
  - Salzmann's nodular 371.46
  - stromal NEC 371.56
- dermatochondrocorneal 371.50
- Duchenne's 359.1
- due to malnutrition 263.9
- Erb's 359.1
- familial
  - hyperplastic periosteal 756.59
  - osseous 277.5
- 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
  - congenital (hereditary) 359.0
    - myotonic 359.22
  - distal 359.1
  - Duchenne's 359.1
  - Erb's 359.1
  - fascioscapulohumeral 359.1
  - Gowers' 359.1
  - hereditary (progressive) 359.1
  - Landouzy-Déjérine 359.1
  - limb-girdle 359.1
  - myotonic 359.21
  - progressive (hereditary) 359.1
    - Charcôt-Marie-Tooth 356.1
  - pseudohypertrophic (infantile) 359.1
- myocardium, myocardial (see also Degeneration, myocardial) 429.1
- myotonic 359.21
- myotonica 359.21
- nail 703.8
  - congenital 757.5
- 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
- reflex neuromuscular - see Dystrophy, sympathetic
- retina, retinal (hereditary) 362.70
  - albipunctate 362.74
  - Bruch's membrane 362.77
  - cone, progressive 362.75
  - hyaline 362.77
  - in
    - Bassen-Kornzweig syndrome 272.5 [362.72]
    - cerebroretinal lipidosis 330.1 [362.71]
    - Refsum's disease 356.3 [362.72]
    - systemic lipidosis 272.7 [362.71]
  - juvenile (Stargardt's) 362.75
  - pigmentary 362.74
  - pigment epithelium 362.76
  - progressive cone (-rod) 362.75
  - pseudoinflammatory foveal 362.77
  - rod, progressive 362.75
  - sensory 362.75
  - vitelliform 362.76
- Salzmann's nodular 371.46
- scapuloperoneal 359.1
- skin NEC 709.9
- sympathetic (posttraumatic) (reflex) 337.20
  - lower limb 337.22
  - specified site NEC 337.29
  - upper limb 337.21
- tapetoretinal NEC 362.74
- thoracic asphyxiating 756.4
- unguium 703.8
  - congenital 757.5
- vitreoretinal (primary) 362.73
  - secondary 362.66
- 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

783.7

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784

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 783.9 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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