Convert to ICD-10-CM:
759.0 converts approximately to:
- 2015/16 ICD-10-CM Q89.01 Asplenia (congenital)
Or:
- 2015/16 ICD-10-CM Q89.09 Congenital malformations of spleen
ICD-9-CM Volume 2 Index entries containing back-references to
759.0:
- Aberrant (congenital) - see also Malposition, congenital
- spleen 759.0
- Absence (organ or part) (complete or partial)
- spleen (congenital) 759.0
- Accessory (congenital)
- spleen 759.0
- Agenesis - see also Absence, by site, congenital
- spleen 759.0
- Anomaly, anomalous (congenital) (unspecified type) 759.9
- specified type NEC
- adrenal (gland) 759.1
- alimentary tract (complete) (partial) 751.8
- ankle 755.69
- anus, anal (canal) 751.5
- aorta, aortic 747.29
- appendix 751.5
- arm 755.59
- artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- auditory canal 744.29
- causing impairment of hearing 744.02
- bile duct or passage 751.69
- bladder 753.8
- bone(s) 756.9
- brain 742.4
- breast 757.6
- broad ligament 752.19
- bronchus 748.3
- canal of Nuck 752.89
- cardiac septal closure 745.8
- carpus 755.59
- cartilaginous 756.9
- cecum 751.5
- cervix 752.49
- chest (wall) 756.3
- chin 744.89
- ciliary body 743.46
- circulatory system 747.89
- clavicle 755.51
- clitoris 752.49
- coccyx 756.19
- colon 751.5
- common duct 751.69
- connective tissue 756.89
- cricoid cartilage 748.3
- cystic duct 751.69
- diaphragm 756.6
- digestive organ(s) or tract 751.8
- duodenum 751.5
- ear 744.29
- auricle 744.29
- causing impairment of hearing 744.02
- causing impairment of hearing 744.09
- inner (causing impairment of hearing) 744.05
- middle, except ossicles 744.03
- ejaculatory duct 752.89
- endocrine 759.2
- epiglottis 748.3
- esophagus 750.4
- Eustachian tube 744.24
- eye 743.8
- face 744.89
- fallopian tube 752.19
- fascia 756.89
- femur 755.69
- fibula 755.69
- finger 755.59
- foot 755.67
- fovea centralis 743.55
- gallbladder 751.69
- Gartner's duct 752.89
- gastrointestinal tract 751.8
- genitalia, genital organ(s)
- genitourinary tract NEC 752.89
- glottis 748.3
- hair 757.4
- hand 755.59
- heart 746.89
- hepatic duct 751.69
- hydatid of Morgagni 752.89
- hymen 752.49
- integument 757.8
- intestine (large) (small) 751.5
- iris 743.46
- jejunum 751.5
- joint 755.8
- kidney 753.3
- knee 755.64
- labium (majus) (minus) 752.49
- labyrinth, membranous 744.05
- larynx 748.3
- leg 755.69
- lens 743.39
- limb, except reduction deformity 755.8
- lower 755.69
- reduction deformity (see also Deformity, reduction, lower limb) 755.30
- upper 755.59
- reduction deformity (see also Deformity, reduction, upper limb) 755.20
- lip 750.26
- liver 751.69
- lung (fissure) (lobe) 748.69
- meatus urinarius 753.8
- metacarpus 755.59
- mouth 750.26
- Müllerian
- muscle 756.89
- musculoskeletal system, except limbs 756.9
- nail 757.5
- neck 744.89
- nerve 742.8
- nervous system 742.8
- nipple 757.6
- nose 748.1
- organ NEC 759.89
- osseous meatus (ear) 744.03
- ovary 752.0
- oviduct 752.19
- pancreas 751.7
- parathyroid 759.2
- patella 755.64
- pelvic girdle 755.69
- penis 752.69
- pericardium 746.89
- peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
- pharynx 750.29
- pituitary 759.2
- prostate 752.89
- radius 755.59
- rectum 751.5
- respiratory system 748.8
- rib 756.3
- round ligament 752.89
- sacrum 756.19
- salivary duct or gland 750.26
- scapula 755.59
- sclera 743.47
- scrotum 752.89
- seminal duct or tract 752.89
- shoulder girdle 755.59
- site NEC 759.89
- skin 757.39
- skull (bone(s)) 756.0
- specified organ or site NEC 759.89
- spermatic cord 752.89
- spinal cord 742.59
- spine 756.19
- spleen 759.0
- sternum 756.3
- stomach 750.7
- tarsus 755.67
- tendon 756.89
- testis 752.89
- thorax (wall) 756.3
- thymus 759.2
- thyroid (gland) 759.2
- tibia 755.69
- toe 755.66
- tongue 750.19
- trachea (cartilage) 748.3
- ulna 755.59
- urachus 753.7
- ureter 753.4
- urethra 753.8
- urinary tract 753.8
- uterus (Müllerian) 752.39
- uvula 750.26
- vagina 752.49
- vascular NEC (see also Anomaly, peripheral vascular system) 747.60
- vas deferens 752.89
- vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- vena cava (inferior) (superior) 747.49
- vertebra 756.19
- vulva 752.49
- spleen 759.0
- Aplasia - see also Agenesis
- spleen 759.0
- Asplenia 759.0
- Cyst (mucus) (retention) (serous) (simple)
- spleen NEC 289.59
- congenital 759.0
- hydatid (see also Echinococcus) 122.9
- Deformity 738.9
- spleen
- acquired 289.59
- congenital 759.0
- Disease, diseased - see also Syndrome
- polycystic (congenital) 759.89
- spleen (organic) (postinfectional) 289.50
- Displacement, displaced
- spleen, congenital 759.0
- Distortion (congenital)
- spleen 759.0
- Ectopic, ectopia (congenital) 759.89
- spleen 759.0
- Enlargement, enlarged - see also Hypertrophy
- spleen (see also Splenomegaly) 789.2
- congenital 759.0
- Hypoplasia, hypoplasis 759.89
- spleen 759.0
- Ivemark's syndrome (asplenia with congenital heart disease) 759.0
- Lobulation (congenital) - see also Anomaly, specified type NEC, by site
- spleen 759.0
- Malposition
- congenital
- adrenal (gland) 759.1
- alimentary tract 751.8
- aorta 747.21
- appendix 751.5
- arterial trunk 747.29
- artery (peripheral) NEC (see also Malposition, congenital, peripheral vascular system) 747.60
- auditory canal 744.29
- causing impairment of hearing 744.02
- auricle (ear) 744.29
- biliary duct or passage 751.69
- bladder (mucosa) 753.8
- exteriorized or extroverted 753.5
- brachial plexus 742.8
- brain tissue 742.4
- breast 757.6
- bronchus 748.3
- cardiac apex 746.87
- cecum 751.5
- clavicle 755.51
- colon 751.5
- digestive organ or tract NEC 751.8
- ear (auricle) (external) 744.29
- endocrine (gland) NEC 759.2
- epiglottis 748.3
- Eustachian tube 744.24
- eye 743.8
- facial features 744.89
- fallopian tube 752.19
- finger(s) 755.59
- foot 755.67
- gallbladder 751.69
- gastrointestinal tract 751.8
- genitalia, genital organ(s) or tract
- glottis 748.3
- hand 755.59
- heart 746.87
- dextrocardia 746.87
- with complete transposition of viscera 759.3
- hepatic duct 751.69
- hip (joint) (see also Dislocation, hip, congenital) 754.30
- intestine (large) (small) 751.5
- with anomalous adhesions, fixation, or malrotation 751.4
- joint NEC 755.8
- kidney 753.3
- larynx 748.3
- limb 755.8
- liver 751.69
- lung (lobe) 748.69
- nail(s) 757.5
- nerve 742.8
- nervous system NEC 742.8
- nose, nasal (septum) 748.1
- organ or site NEC - see Anomaly, specified type NEC, by site
- ovary 752.0
- pancreas 751.7
- parathyroid (gland) 759.2
- patella 755.64
- peripheral vascular system 747.60
- pituitary (gland) 759.2
- respiratory organ or system NEC 748.9
- rib (cage) 756.3
- supernumerary in cervical region 756.2
- scapula 755.59
- shoulder 755.59
- spinal cord 742.59
- spine 756.19
- spleen 759.0
- sternum 756.3
- stomach 750.7
- symphysis pubis 755.69
- testis (undescended)752.51
- thymus (gland) 759.2
- thyroid (gland) (tissue) 759.2
- toe(s) 755.66
- tongue 750.19
- trachea 748.3
- uterus 752.39
- vein(s) (peripheral) NEC (see also Malposition, congenital, peripheral vascular system) 747.60
- vena cava (inferior) (superior) 747.49
- Polycystic (congenital) (disease) 759.89
- spleen 759.0
- Polysplenia syndrome 759.0
- Spleen, splenic - see also condition
- agenesis 759.0
- Splenomegaly 789.2
- congenital 759.0
- Supernumerary (congenital)
- spleen 759.0
- Syndrome - see also Disease
- Ivemark's (asplenia with congenital heart disease) 759.0
- polysplenia 759.0
- splenic