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Draft ICD-10-CM/PCS MS-DRGv30.0 Definitions Manual Previous Page [Alt-p] Up a level [Alt-u] Next Page [Alt-n]
Appendix C: Principal diagnoses which convert CC/MCC to non-CC
PDX Collection 1038:35 codes (continued)
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1039:84 codes
D500Iron deficiency anemia secondary to blood loss (chronic)
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D550Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551Anemia due to other disorders of glutathione metabolism
D552Anemia due to disorders of glycolytic enzymes
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D564Hereditary persistence of fetal hemoglobin [HPFH]
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D57211Sickle-cell/Hb-C disease with acute chest syndrome
D57212Sickle-cell/Hb-C disease with splenic sequestration
D57219Sickle-cell/Hb-C disease with crisis, unspecified
D573Sickle-cell trait
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D580Hereditary spherocytosis
D581Hereditary elliptocytosis
D582Other hemoglobinopathies
D588Other specified hereditary hemolytic anemias
D589Hereditary hemolytic anemia, unspecified
D590Drug-induced autoimmune hemolytic anemia
D591Other autoimmune hemolytic anemias
D592Drug-induced nonautoimmune hemolytic anemia
D593Hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D630Anemia in neoplastic disease
D631Anemia in chronic kidney disease
D638Anemia in other chronic diseases classified elsewhere
D640Hereditary sideroblastic anemia
D641Secondary sideroblastic anemia due to disease
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D759Disease of blood and blood-forming organs, unspecified
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
 
PDX Collection 1040:62 codes
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D564Hereditary persistence of fetal hemoglobin [HPFH]
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D573Sickle-cell trait
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D582Other hemoglobinopathies
D590Drug-induced autoimmune hemolytic anemia
D591Other autoimmune hemolytic anemias
D593Hemolytic-uremic syndrome
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D630Anemia in neoplastic disease
D631Anemia in chronic kidney disease
D638Anemia in other chronic diseases classified elsewhere
D640Hereditary sideroblastic anemia
D641Secondary sideroblastic anemia due to disease
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D759Disease of blood and blood-forming organs, unspecified
P615Transient neonatal neutropenia
P618Other specified perinatal hematological disorders
P619Perinatal hematological disorder, unspecified
 
PDX Collection 1041:39 codes
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P700Syndrome of infant of mother with gestational diabetes
P701Syndrome of infant of a diabetic mother
P702Neonatal diabetes mellitus
P703Iatrogenic neonatal hypoglycemia
P704Other neonatal hypoglycemia
P709Transitory disorder of carbohydrate metabolism of newborn, unspecified
P710Cow's milk hypocalcemia in newborn
P711Other neonatal hypocalcemia
P712Neonatal hypomagnesemia
P713Neonatal tetany without calcium or magnesium deficiency
P714Transitory neonatal hypoparathyroidism
P718Other transitory neonatal disorders of calcium and magnesium metabolism
P719Transitory neonatal disorder of calcium and magnesium metabolism, unspecified
P721Transitory neonatal hyperthyroidism
P729Transitory neonatal endocrine disorder, unspecified
P740Late metabolic acidosis of newborn
P741Dehydration of newborn
P742Disturbances of sodium balance of newborn
P743Disturbances of potassium balance of newborn
P744Other transitory electrolyte disturbances of newborn
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1042:22 codes
P700Syndrome of infant of mother with gestational diabetes
P701Syndrome of infant of a diabetic mother
P702Neonatal diabetes mellitus
P703Iatrogenic neonatal hypoglycemia
P704Other neonatal hypoglycemia
P709Transitory disorder of carbohydrate metabolism of newborn, unspecified
P710Cow's milk hypocalcemia in newborn
P711Other neonatal hypocalcemia
P712Neonatal hypomagnesemia
P713Neonatal tetany without calcium or magnesium deficiency
P714Transitory neonatal hypoparathyroidism
P718Other transitory neonatal disorders of calcium and magnesium metabolism
P719Transitory neonatal disorder of calcium and magnesium metabolism, unspecified
P721Transitory neonatal hyperthyroidism
P729Transitory neonatal endocrine disorder, unspecified
P740Late metabolic acidosis of newborn
P741Dehydration of newborn
P742Disturbances of sodium balance of newborn
P743Disturbances of potassium balance of newborn
P744Other transitory electrolyte disturbances of newborn
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
 
PDX Collection 1043:18 codes
P760Meconium plug syndrome
P761Transitory ileus of newborn
P762Intestinal obstruction due to inspissated milk
P768Other specified intestinal obstruction of newborn
P769Intestinal obstruction of newborn, unspecified
P771Stage 1 necrotizing enterocolitis in newborn
P772Stage 2 necrotizing enterocolitis in newborn
P773Stage 3 necrotizing enterocolitis in newborn
P779Necrotizing enterocolitis in newborn, unspecified
P780Perinatal intestinal perforation
P781Other neonatal peritonitis
P782Neonatal hematemesis and melena due to swallowed maternal blood
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7889Other specified perinatal digestive system disorders
P789Perinatal digestive system disorder, unspecified
 
PDX Collection 1044:35 codes
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P760Meconium plug syndrome
P761Transitory ileus of newborn
P762Intestinal obstruction due to inspissated milk
P768Other specified intestinal obstruction of newborn
P769Intestinal obstruction of newborn, unspecified
P771Stage 1 necrotizing enterocolitis in newborn
P772Stage 2 necrotizing enterocolitis in newborn
P773Stage 3 necrotizing enterocolitis in newborn
P779Necrotizing enterocolitis in newborn, unspecified
P780Perinatal intestinal perforation
P781Other neonatal peritonitis
P782Neonatal hematemesis and melena due to swallowed maternal blood
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7889Other specified perinatal digestive system disorders
P789Perinatal digestive system disorder, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1045:3 codes
P830Sclerema neonatorum
P8330Unspecified edema specific to newborn
P8339Other edema specific to newborn
 
PDX Collection 1046:18 codes
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P832Hydrops fetalis not due to hemolytic disease
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1047:9 codes
P800Cold injury syndrome
P808Other hypothermia of newborn
P809Hypothermia of newborn, unspecified
P810Environmental hyperthermia of newborn
P818Other specified disturbances of temperature regulation of newborn
P819Disturbance of temperature regulation of newborn, unspecified
P830Sclerema neonatorum
P8330Unspecified edema specific to newborn
P8339Other edema specific to newborn
 
PDX Collection 1048:20 codes
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P90Convulsions of newborn
P918Other specified disturbances of cerebral status of newborn
P919Disturbance of cerebral status of newborn, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1049:8 codes
P90Convulsions of newborn
P910Neonatal cerebral ischemia
P911Acquired periventricular cysts of newborn
P913Neonatal cerebral irritability
P914Neonatal cerebral depression
P915Neonatal coma
P918Other specified disturbances of cerebral status of newborn
P919Disturbance of cerebral status of newborn, unspecified
 
PDX Collection 1050:5 codes
P84Other problems with newborn
P9160Hypoxic ischemic encephalopathy [HIE], unspecified
P9161Mild hypoxic ischemic encephalopathy [HIE]
P9162Moderate hypoxic ischemic encephalopathy [HIE]
P9163Severe hypoxic ischemic encephalopathy [HIE]
 
PDX Collection 1051:2 codes
P9201Bilious vomiting of newborn
P9209Other vomiting of newborn
 
PDX Collection 1052:4 codes
P930Grey baby syndrome
P938Other reactions and intoxications due to drugs administered to newborn
P961Neonatal withdrawal symptoms from maternal use of drugs of addiction
P962Withdrawal symptoms from therapeutic use of drugs in newborn
 
PDX Collection 1053:3 codes
Q000Anencephaly
Q001Craniorachischisis
Q002Iniencephaly
 
PDX Collection 1054:14 codes
Q010Frontal encephalocele
Q011Nasofrontal encephalocele
Q012Occipital encephalocele
Q018Encephalocele of other sites
Q019Encephalocele, unspecified
Q02Microcephaly
Q040Congenital malformations of corpus callosum
Q041Arhinencephaly
Q042Holoprosencephaly
Q043Other reduction deformities of brain
Q044Septo-optic dysplasia of brain
Q045Megalencephaly
Q046Congenital cerebral cysts
Q048Other specified congenital malformations of brain
 
PDX Collection 1055:4 codes
Q044Septo-optic dysplasia of brain
Q045Megalencephaly
Q046Congenital cerebral cysts
Q048Other specified congenital malformations of brain



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