2008 ICD-9-CM Diagnosis Code 783.9 : Other symptoms concerning nutrition metabolism and development

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2008 ICD-9-CM Diagnosis Code 783.9

Other symptoms concerning nutrition metabolism and development

783.7

784

783.9 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 783.9: 2009 2010

Excludes

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 783.9 Click to expand

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
  - 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
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

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