In
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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