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FETAL ICD-10 CODES QUICK REFERENCE GUIDE

FETAL ICD-10 CODESQUICK REFERENCE GUIDE Page CONTENTS 1 Cardiac Anomalies 3 Chromosome Abnormalities 4 Central Nervous System Anomalies5 Extremity Anomalies 6 Face / Neck Anomalies7 Gastrointestinal Anomalies7 Pulmonary Anomalies7 Renal Anomalies8 Skeletal DysplasiaICD-10-CM Coding Rules All FETAL anomaly CODES begin with a maternal code followed by a FETAL code . All of the leading CODES begin with the letter O and not the number zero. Maternal Category O35 is used to designate maternal care for known or suspected FETAL abnormality and damage. Where applicable, a 7th character is to be assigned to the maternal code to identify the fetus for which the complication code applies. DISCLAIMER: The FETAL ICD-10 QUICK REFERENCE GUIDE is intended to serve as a resource but should not take place of personal verification of all CODES when used for billing purposes. FETAL CARDIAC ANOMALIES ABNORMAL CONNECTIONS Atrial isomerism arterial trunk transposition of great vessels inlet ventricle outlet left ventricle outlet right ventricle image atrial arrangement of great vessels AORTIC/MITRAL VALVES Aortic arch hypoplasia (w/HLHS) valve atresia valve insufficiency valve stenosis aortic valve left heart syndrome atresia stenosis valve insufficiency malformations; aortic or mitral valve SEPTAL ANOMALIES Aortopulmonary septal defect septal defect AV canal primum defect of Fallot septal defect A

Page CONTENTS 1 Cardiac Anomalies 3 Chromosome Abnormalities 4 Central Nervous System Anomalies 5 Extremity Anomalies 6 Face / Neck Anomalies 7 Gastrointestinal Anomalies 7 Pulmonary Anomalies 7 Renal Anomalies 8 Skeletal Dysplasia ICD-10-CM Coding Rules • All fetal anomaly codes begin with a maternal code followed by a fetal code. • All of the leading codes begin with the letter

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Transcription of FETAL ICD-10 CODES QUICK REFERENCE GUIDE

1 FETAL ICD-10 CODESQUICK REFERENCE GUIDE Page CONTENTS 1 Cardiac Anomalies 3 Chromosome Abnormalities 4 Central Nervous System Anomalies5 Extremity Anomalies 6 Face / Neck Anomalies7 Gastrointestinal Anomalies7 Pulmonary Anomalies7 Renal Anomalies8 Skeletal DysplasiaICD-10-CM Coding Rules All FETAL anomaly CODES begin with a maternal code followed by a FETAL code . All of the leading CODES begin with the letter O and not the number zero. Maternal Category O35 is used to designate maternal care for known or suspected FETAL abnormality and damage. Where applicable, a 7th character is to be assigned to the maternal code to identify the fetus for which the complication code applies. DISCLAIMER: The FETAL ICD-10 QUICK REFERENCE GUIDE is intended to serve as a resource but should not take place of personal verification of all CODES when used for billing purposes. FETAL CARDIAC ANOMALIES ABNORMAL CONNECTIONS Atrial isomerism arterial trunk transposition of great vessels inlet ventricle outlet left ventricle outlet right ventricle image atrial arrangement of great vessels AORTIC/MITRAL VALVES Aortic arch hypoplasia (w/HLHS) valve atresia valve insufficiency valve stenosis aortic valve left heart syndrome atresia stenosis valve insufficiency malformations.

2 Aortic or mitral valve SEPTAL ANOMALIES Aortopulmonary septal defect septal defect AV canal primum defect of Fallot septal defect ARTERIES Aneurysmal arterial duct arch hypoplasia (isolated) atresia dilation stenosis of the aorta aortic arch artery atresia artery stenosis sided aortic arch ring anomaly GREAT VEINS Absent ductus venosus anomalous pulmonary veins azygous vein left superior vena cava anomalous pulmonary veins PULMONARY/TRICUSPID VALVES Ebstein s anomaly right heart syndrome malformations, pulmonary valve malformations, tricuspid valve valve atresia valve regurgitation valve stenosis atresia regurgitation stenosis VENTRICLES Congenital heart block fibroelastosis myocardium aneurysm DISTURBANCES Atrial flutter premature beats heart block sinus syndrome bradycardia tachycardia premature beats tachycardia FETAL CHROMOSOME ABNORMALITIES MONOSOMIES Monosomy, nonmosaicisim , mosaicism SEX CHROMOSOMES 45 X (Turner s)

3 X, iso , XXX , XXY , XYY 45 X, 46 XX or XY Triploidy 13 13, mosaic 13, translocation 18 18, mosaic 18, translocation 21 21, mosaic 21, translocation autosomal trisomy autosomal trisomy, mosaic autosomal trisomy, partial CHROMOSOMES Balanced rearrangement, abnormal phenotype rearrangement, normal phenotype X FETAL CENTRAL NERVOUS SYSTEM ANOMALIES CENTRAL DEFECTS Agenesis of the corpus callosum dysplasia of Galen aneurysm CRANIAL Acrania (other) encephalocele encephalocele HYDROCEPHALUS Aqueductal stenosis hydrocephalus, other MIGRATION PROBLEMS Agenesis of the corpus callosum POSTERIOR FOSSA Cerebellar hypoplasia cyst variant cisterna magnae hypoplasia/agenesis FETAL EXTREMITY ANOMALIES FOOT Absent foot and toes, bilateral foot and toes, left foot and toes, right , both feet , left foot , right foot calcaneovalgus calcaneovarus equinovarus HAND Absent hand and fingers, bilateral hand and fingers, left hand and fingers, right , both hands , left hand , right hand LOWER EXTREMITY Absence of leg (foot present), bilateral of leg (foot present), left of leg (foot present)

4 , right of limb, bilateral of limb, left of limb, right of lower leg and foot, bilateral of lower leg and foot, left of lower leg and foot, right of femur of tibia/fibula defect of femur, bilateral defect of femur, left defect of femur, right of fibula, bilateral of fibula, left of fibula, right of tibia, bilateral of tibia, left of tibia, right UPPER EXTREMITY Absence of arm (hand present), bilateral of arm (hand present), left of arm (hand present), right of forearm and hand, bilateral of forearm and hand, left of forearm and hand, right of limb, bilateral of limb, left of limb, right of long bone of radius, bilateral of radius, left of radius, right of ulna, bilateral of ulna, left of ulna, right of upper limb, bilateral of upper limb, left of upper limb, right FETAL FACE/NECK ANOMALIES Cervical teratoma hard and soft palate hard palate lip bilateral/cleft palate lip unilateral/cleft palate lip, bilateral lip, median lip, unilateral FETAL GASTROINTESTINAL ANOMALIES Absent diaphragm atresia hernia atresia atresia of diaphragm duplication cyst inversus bowel obstruction stomach fistula FETAL PULMONARY ANOMALIES Bronchial atresia sequestration FETAL RENAL ANOMALIES Horseshoe kidney polycystic kidney kidney agenesis, bilateral agenesis, unilateral hypoplasia, bilateral hypoplasia.

5 Unilateral Extrophy of bladder, cloacal of bladder, unspecified urethral valves belly syndrome duplication obstruction obstruction GENITALIA Ambiguous genitalia stricture SKELETAL DYSPLASIAS Achondroplasia dysplasia imperfecta rib syndrome dysplasia skeletal dysplasia FETAL SPINE ANOMALIES Arnold-Chiari w/hydrocephalus w/spina bifida w/spina bifida and hydrocephalus SB w/hydrocephalus SB w/o hydrocephalus (cervical) (cerv-thoracic) (thoracic) (thoraco-lumbar) (unspecified) SB w/hydrocephalus SB w/o hydrocephalus SB w/hydrocephalus SB w/o hydrocephalus teratoma calcaneovalgus calcaneovarus equinovarus SB w/hydrocephalus SB w/o hydrocephalus SB w/hydrocephalus FETAL Center at Children s Memorial Hermann Hospital, affiliated with the physicians at McGovern Medical School at UTHealth, is a national leader in FETAL diagnosis, FETAL intervention and com-prehensive FETAL care for babies with congenital anomalies or genetic abnormalities requiring treatment before or after birth.

6 A national referring center, The FETAL Center offers patients a complete range of prenatal testing and FETAL interventions with a multidisciplinary, coordinated program for mother and child before, during and after birth. Contact Us: Call: : FETAL Center6410 Fannin, Suite 210 Houston, TX 77030