DRAFT

ICD-10-CM/PCS MS-DRG v44.0 Definitions Manual
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Appendix C: Principal Diagnoses which Convert CC/MCC to non-CC
Page 328 of 453
PDX Collection 1483 (continued)
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
QA00142DLG4-related synaptopathy
QA00149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA00151FOXG1 syndrome
QA00159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA08Other neurodevelopmental disorders related to pathogenic variants in other specific genes
 
PDX Collection 1484
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q224Congenital tricuspid stenosis
Q225Ebstein's anomaly
Q226Hypoplastic right heart syndrome
Q228Other congenital malformations of tricuspid valve
Q229Congenital malformation of tricuspid valve, unspecified
Q230Congenital stenosis of aortic valve
Q231Congenital insufficiency of aortic valve
Q232Congenital mitral stenosis
Q233Congenital mitral insufficiency
Q234Hypoplastic left heart syndrome
Q2381Bicuspid aortic valve
Q2382Congenital mitral valve cleft leaflet
Q2388Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan syndrome, unspecified
Q87410Marfan syndrome with aortic dilation
Q87418Marfan syndrome with other cardiovascular manifestations
Q8742Marfan syndrome with ocular manifestations
Q8743Marfan syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q992Fragile X chromosome
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
QA00142DLG4-related synaptopathy
QA00149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA00151FOXG1 syndrome
QA00159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA08Other neurodevelopmental disorders related to pathogenic variants in other specific genes
 
PDX Collection 1485
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q224Congenital tricuspid stenosis
Q225Ebstein's anomaly
Q226Hypoplastic right heart syndrome
Q228Other congenital malformations of tricuspid valve
Q229Congenital malformation of tricuspid valve, unspecified
Q230Congenital stenosis of aortic valve
Q231Congenital insufficiency of aortic valve
Q232Congenital mitral stenosis
Q233Congenital mitral insufficiency
Q234Hypoplastic left heart syndrome
Q2381Bicuspid aortic valve
Q2382Congenital mitral valve cleft leaflet
Q2388Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan syndrome, unspecified
Q87410Marfan syndrome with aortic dilation
Q87418Marfan syndrome with other cardiovascular manifestations
Q8742Marfan syndrome with ocular manifestations
Q8743Marfan syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q992Fragile X chromosome
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
QA00142DLG4-related synaptopathy
QA00149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA00151FOXG1 syndrome
QA00159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA08Other neurodevelopmental disorders related to pathogenic variants in other specific genes
 
PDX Collection 1486
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q2381Bicuspid aortic valve
Q2382Congenital mitral valve cleft leaflet
Q2388Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q240Dextrocardia
Q241Levocardia
Q242Cor triatriatum
Q243Pulmonary infundibular stenosis
Q244Congenital subaortic stenosis
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
QA00142DLG4-related synaptopathy
QA00149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA00151FOXG1 syndrome
QA00159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA08Other neurodevelopmental disorders related to pathogenic variants in other specific genes
 
PDX Collection 1487
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q2381Bicuspid aortic valve
Q2382Congenital mitral valve cleft leaflet
Q2388Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q242Cor triatriatum
Q243Pulmonary infundibular stenosis
Q244Congenital subaortic stenosis
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan syndrome, unspecified
Q87410Marfan syndrome with aortic dilation
Q87418Marfan syndrome with other cardiovascular manifestations
Q8742Marfan syndrome with ocular manifestations
Q8743Marfan syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q992Fragile X chromosome
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
QA00142DLG4-related synaptopathy
QA00149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA00151FOXG1 syndrome
QA00159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA08Other neurodevelopmental disorders related to pathogenic variants in other specific genes
 
PDX Collection 1488
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q2381Bicuspid aortic valve
Q2382Congenital mitral valve cleft leaflet
Q2388Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q245Malformation of coronary vessels
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
 
PDX Collection 1489
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q2381Bicuspid aortic valve
Q2382Congenital mitral valve cleft leaflet
Q2388Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q246Congenital heart block
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan syndrome, unspecified
Q87410Marfan syndrome with aortic dilation
Q87418Marfan syndrome with other cardiovascular manifestations
Q8742Marfan syndrome with ocular manifestations
Q8743Marfan syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q992Fragile X chromosome
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
QA00142DLG4-related synaptopathy
QA00149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
QA00151FOXG1 syndrome
QA00159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
QA08Other neurodevelopmental disorders related to pathogenic variants in other specific genes
 
PDX Collection 1490
Q250Patent ductus arteriosus
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
 
PDX Collection 1491
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q251Coarctation of aorta
Q2521Interruption of aortic arch
Q2529Other atresia of aorta
Q253Supravalvular aortic stenosis
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8786Kleefstra syndrome
Q8787Hao-Fountain Syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q87ALoeys-Dietz syndrome
Q897Multiple congenital malformations, not elsewhere classified
Q8981Kabuki syndrome
Q8989Other specified congenital malformations
Q99811Usher syndrome, type 1
Q99812Usher syndrome, type 2
Q99813Usher syndrome, type 3
Q99818Other Usher syndrome
Q99819Usher syndrome, unspecified
QA00101SCN2A-related neurodevelopmental disorder
QA00102CACNA1A-related neurodevelopmental disorder
QA00109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
QA0011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
QA0012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
QA00131SLC6A1-related disorder
QA00139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
QA00141Syntaxin-binding protein 1-related disorder
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