Indiana Administrative Code
Title 410 - INDIANA DEPARTMENT OF HEALTH
Article 21 - REPORTING
Rule 3 - Birth Problems Registry
Section 3-9 - Reportable birth problems
Universal Citation: 410 IN Admin Code 3-9
Current through March 20, 2024
Authority: IC 16-38-4-7
Affected: IC 16-38-4
Sec. 9.
The following categories along with those conditions identified in the International Classification of Diseases - Ninth Revision, Clinical Modification, 1998 (ICD-9-CM) are birth problems:
(1) A structural deformation.
(2) A developmental malformation.
(3) A genetic, inherited, or biochemical disease.
(4) A condition of a chronic nature, including:
(A) central nervous
system hemorrhage; or
(B) infection
of the central nervous system;
that may result in a need for long term health care.
(5) A pervasive developmental disorder.
(6) A fetal alcohol spectrum disorder.
(7) Any other severe disability that is recognized:
(A) in a child
after birth; and
(B) before the
child becomes three (3) years of age.
(8)
| ICD-9-CM Codes | Name |
| 155-208 | Neoplasms |
| 216-216.9 | Neoplasms |
| 230-234 | Neoplasms |
| 246.1 | Dyshormonogenic goiter |
| 250 | Diabetes mellitus |
| 257.8 | Other testicular dysfunction |
| 279 | Disorders involving the immune mechanism |
| 282 | Hereditary hemolytic anemias |
| 284.0 | Constitutional aplastic anemia |
| 286.0-286.5 | Coagulation defects |
| 287.3 | Primary thrombocytopenia |
| 288 | Diseases of white blood cells |
| 289.6 | Familial polycythemia |
| 299.00-299.99 | Pervasive developmental disorders including autism, childhood disintegrative disorder, Asperger's syndrome, Rett syndrome, and pervasive developmental disorders not otherwise specified |
| 330 | Cerebral degenerations usually manifest childhood |
| 335 | Anterior horn cell disease |
| 359 | Muscular dystrophies and myopathies |
| 362.21 | Retrolental fibroplasia |
| 362.7 | Hereditary retinal dystrophies |
| 365.14 | Glaucoma of childhood |
| 378 | Strabismus and other disorders of binocular eye movement |
| 379.51 | Congenital nystagmus |
| 389.0-389.9 | Hearing loss |
| 524.0-524.1 | Anomalies of jaw Congenital anomalies |
| 740-742 | Central nervous system |
| 743-744 | Orofacial |
| 745-747 | Cardiovascular |
| 748 | Respiratory |
| 749-750.29 | Orofacial |
| 750.3-751 | Gastrointestinal |
| 752-753 | Genitourinary |
| 754-756 | Musculoskeletal |
| 757 | Integument |
| 758 | Chromosome and syndromes |
| 759 | Other and unspecified congenital anomalies |
| 760.71 | Fetal alcohol syndrome |
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