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Reportable Conditions List (Organized Numerically by ICD-10-CM Code)

ICD-10-CM Diagnosis Codes Categories of Congenital Anomalies

F84.0 – F84.9* Pervasive developmental disorders (includes autism, childhood disintegrative disorder, Asperger’s, & Rett syndrome; reported at any age)

Q00.0 – Q07.9, G90.1 Central nervous system

Q10.0 – Q18.9, Q35.1 – Q38.8 Orofacial

Q20.0 – Q28.9, P29.3 Cardiovascular

Q30.0 – Q34.9 Respiratory

Q39.0 – Q45.9 Gastrointestinal

Q50.01 – Q64.9 Genitourinary

Q65.00 – Q79.9 Musculoskeletal

Q80.0 – Q84.9 Integument

Q85.0 – Q89.9, E78.71, E78.72 Congenital anomalies, other & unspecified

Q86.0, P04.3* Fetal alcohol syndrome (reported up to 5 years)

Q90.0 – Q99.9 Chromosome & syndromes

ICD-10-CM Diagnosis Codes Other Reportable Conditions

C00.0 – C41.9 Neoplasms

C88.0 Waldenstrom’s macroglobulinemia

D47.4, D75.81 – D75.89, D89.2 Thrombophilias

D55.0 – D58.9 Hereditary hemolytic anemias

D61.0 – D61.8 Constitutional aplastic anemia

D66, D67, D68.0 – D68.9 Coagulation defects

D69.3 – D69.42 Primary thrombocytopenia

D70.0 – D76.3 White blood cell diseases

D75.0 Familial polycythemia

D75.81 – D75.89 Other specified diseases of blood & blood-forming organs

D80.0 – D89.9 Immune mechanism disorders

E00.0 – E00.9, E07.89, E25.0 – E25.9 Endocrine newborn screening conditions

E03.4, E07.89 Thyroid-binding globulin deficiency

E07.1, E07.9 Dyshormonogenic goiter

E10 – E11.9 Diabetes mellitus

E29.8 Testicular dysfunction, other

E70.0 – E74.9, E77.1, E80.3, E88.40 – E88.49, Metabolic newborn screening conditions

C96.5, - C96.6, D81.810 – D81.819,

H49.811 – H49.819

E75.00 – E75.29, G31.81, G31.82, G93.9, G94 Cerebral degenerations usually manifesting in childhood

E76.01 – E76.3 Mucopolysaccharidoses

E84.0 – E84.9 Cystic fibrosis

G12.0 – G12.9 Anterior horn cell disease

G71.0 – G73.7 Muscular dystrophies

H35.179 Retrolental fibroplasia

H35.50 – H35.54 Hereditary retinal dystrophies

H47.61 – H47.619 Cortical blindness

H49.00 – H51.9 Strabismus & other disorders of binocular eye movement

H54.0 – H54.3 Visual impairment

H54.8 Legal blindness, as defined in USA

H55.01 Congenital nystagmus

H90.0 – H91.93 Hearing loss

K40.0 – K40.91 Inguinal hernia

K42.0 – K42.9 Umbilical hernia

P02.8, P02.9 Amniotic band syndrome

M26.00 – M26.10 Anomalies of jaw

N44.00 – N44.04 Torsion of testes

P00.2, P04.1, P04.9 Fetus/newborn exposure to maternal infection or substance

P35.0 – P37.9, A33 Congenital infections

For additional information, please visit: birthdefects.

Updated 12/19/2014

Reportable Conditions List (Organized Alphabetically)

ICD-10-CM Diagnosis Codes Categories of Congenital Anomalies

Q20.0 – Q28.9, P29.3 Cardiovascular

Q00.0 – Q07.9, G90.1 Central nervous system

Q90.0 – Q99.9 Chromosome & syndromes

Q85.0 – Q89.9, E78.71, E78.72 Congenital anomalies, other & unspecified

Q86.0, P04.3* Fetal alcohol syndrome (reported up to 5 years)

Q39.0 – Q45.9 Gastrointestinal

Q50.01 – Q64.9 Genitourinary

Q80.0 – Q84.9 Integument

Q65.00 – Q79.9 Musculoskeletal

Q10.0 – Q18.9, Q35.1 – Q38.8 Orofacial

F84.0 – F84.9* Pervasive developmental disorders (includes autism, childhood disintegrative disorder, Asperger’s, & Rett syndrome; reported at any age)

Q30.0 – Q34.9 Respiratory

ICD-10-CM Diagnosis Codes Other Reportable Conditions

P02.8, P02.9 Amniotic band syndrome

M26.00 – M26.10 Anomalies of jaw

G12.0 – G12.9 Anterior horn cell disease

E75.00 – E75.29, G31.81, G31.82, G93.9, G94 Cerebral degenerations usually manifesting in childhood

D66, D67, D68.0 –D68.9 Coagulation defects

P35.0 – P37.9, A33 Congenital infections

H55.01 Congenital nystagmus

D61.0 – D61.8 Constitutional aplastic anemia

H47.61 – H47.619 Cortical blindness

E84.0 – E84.9 Cystic fibrosis

E10 – E11.9 Diabetes mellitus

E07.1, E07.9 Dyshormonogenic goiter

E00.0 – E00.9, E07.89, E25.0 – E25.9 Endocrine newborn screening conditions

D75.0 Familial polycythemia

P00.2, P04.1, P04.9 Fetus/newborn exposure to maternal infection or substance

H90.0 – H91.93 Hearing loss

D55.0 – D58.9 Hereditary hemolytic anemias

H35.50 – H35.54 Hereditary retinal dystrophies

D80.0 – D89.9 Immune mechanism disorders

K40.0 – K40.91 Inguinal hernia

H54.8 Legal blindness, as defined in USA

E70.0 – E74.9, E77.1, E80.3, E88.40 – E88.49, Metabolic newborn screening conditions

C96.5, - C96.6, D81.810 – D81.819,

H49.811 – H49.819

E76.01 – E76.3 Mucopolysaccharidoses

G71.0 – G73.7 Muscular dystrophies

C00.0 – C41.9 Neoplasms

D75.81 – D75.89 Other specified diseases of blood & blood-forming organs

D69.3 – D69.42 Primary thrombocytopenia:

H35.179 Retrolental fibroplasia

H49.00 – H51.9 Strabismus & other disorders of binocular eye movement

E29.8 Testicular dysfunction, other

D47.4, D68.51 – D68.69, D75.81 – D75.89, D89.2 Thrombophilias

N44.00 – N44.04 Torsion of testes

E03.4, E07.89 Thyroid-binding globulin deficiency

K42.0 – K42.9 Umbilical hernia

H54.0 – H54.3 Visual impairment

C88.0 Waldenstrom’s macroglobulinemia

D70.0 – D76.3 White blood cell diseases

For additional information, please visit: birthdefects.

Updated 12/19/2014

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