2006 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.* > 2006 ICD-9-CM Diagnosis 783.9 Other symptoms concerning nutrition metabolism and development View the most recent version of ICD-9-CM 783.9 783.9 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 Alternate Terminology Hypometabolism 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 359.1 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 359.2 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 359.2 progressive (hereditary) 359.1 Charcôt-Marie-Tooth 356.1 pseudohypertrophic (infantile) 359.1 myocardium, myocardial (see also Degeneration, myocardial) 429.1 myotonic 359.2 myotonica 359.2 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 624.0 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