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New York State Department of Health Congenital Malformation RegistryICD10 Reportable Congenital Malformations Coding Manual List of all Reportable MalformationsLast updated 12/01/2015 10/1/20151 Table
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How to fill out congenital malformation registry

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How to fill out congenital malformation registry:

01
Obtain a copy of the congenital malformation registry form. This form can typically be found online or through your local health department.
02
Begin by entering your personal information, including your name, date of birth, and contact information.
03
Provide details about the congenital malformation, including the specific condition, date of diagnosis, and any relevant medical history.
04
If applicable, include information about any medications or treatments that have been received for the congenital malformation.
05
Include information about any genetic testing or counseling that has been done, as well as any family history of congenital malformations.
06
Be thorough and accurate in filling out the registry form, providing as much detail as possible. This will help researchers and healthcare professionals analyze trends and develop appropriate interventions.
07
Once the form is complete, submit it according to the instructions provided. This may involve mailing it to a specific address or submitting it online through a secure portal.

Who needs congenital malformation registry:

01
Healthcare professionals: Congenital malformation registries are often utilized by healthcare professionals to track the occurrence and prevalence of specific malformations in a particular population. This information can inform research, treatment protocols, and public health strategies.
02
Researchers: Congenital malformation registries are valuable tools for researchers studying the causes, risk factors, and outcomes of various malformations. The data collected in these registries can contribute to the development of new treatments and prevention strategies.
03
Families and individuals affected by congenital malformations: Access to a congenital malformation registry can provide families and individuals with valuable information and resources. By understanding the prevalence of specific malformations and connecting with support networks, affected individuals can access the necessary care and support they require.
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Congenital malformation registry is a database that collects information on babies born with physical abnormalities or defects.
Healthcare providers, hospitals, or other medical facilities are typically required to file the congenital malformation registry.
You can fill out the congenital malformation registry by documenting the necessary information about the newborn with malformations and submitting it to the relevant health authorities.
The purpose of congenital malformation registry is to track and monitor the prevalence of birth defects, identify trends, and improve prevention and treatment strategies.
Information such as the type of malformation, date of birth, gender, mother's health history, and any genetic factors must be reported on the congenital malformation registry.
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