icd 10 code for genetic disorder 286.9

286.9 - Coagulat defect NEC/NOS Not Valid for Submission 286.9 is a legacy non-billable code used to specify a medical diagnosis of other and unspecified coagulation defects. This code was replaced on September 30, 2015 by its ICD-10 equivalent.

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What is the ICD-9 code for diagnosis?

ICD-9-CM 286.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 286.0 should only be used for claims with a date of service on or before September 30, 2015.

What is the ICD 10 code for genetic and chromosomal anomalies?

Encounter for other screening for genetic and chromosomal anomalies. Z13.79 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Encntr for oth screening for genetic and chromsoml anomalies The 2018/2019 edition of ICD-10-CM Z13.79 became effective on October 1,...

What is the ICD 10 code for OTH screening for genetic abnormalities?

Short description: Encntr for oth screening for genetic and chromsoml anomalies The 2021 edition of ICD-10-CM Z13.79 became effective on October 1, 2020. This is the American ICD-10-CM version of Z13.79 - other international versions of ICD-10 Z13.79 may differ. The following code (s) above Z13.79 contain annotation back-references

What is the ICD 10 code for coagulation defect?

286.9 is a legacy non-billable code used to specify a medical diagnosis of other and unspecified coagulation defects. This code was replaced on September 30, 2015 by its ICD-10 equivalent.

Where are ICD-10 genetic disorders?

Genetic susceptibility to other disease Z15. 89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM Z15. 89 became effective on October 1, 2021.

What does diagnosis R53 83 mean?

Code R53. 83 is the diagnosis code used for Other Fatigue. It is a condition marked by drowsiness and an unusual lack of energy and mental alertness. It can be caused by many things, including illness, injury, or drugs.

What is the diagnosis code for trisomy 21?

Q90. 0 (Down syndrome, Trisomy 21, nonmosaicism)

What is the code for congenital Afibrinogenemia?

2 Hereditary deficiency of other clotting factors.

Is R53 83 a billable code?

R53. 83 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is R53 81?

R53. 81: “R” codes are the family of codes related to "Symptoms, signs and other abnormal findings" - a bit of a catch-all category for "conditions not otherwise specified". R53. 81 is defined as chronic debility not specific to another diagnosis.

Is Trisomy 21 a disease?

Down syndrome is a genetic disorder. It is also called trisomy 21. It includes certain birth defects, learning problems, and facial features. A child with Down syndrome also may have heart defects and problems with vision and hearing.

What is the ICD-10 code for Down's syndrome?

ICD-10 code Q90. 9 for Down syndrome, unspecified is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

What is the difference between Mosaic Down syndrome and Down syndrome?

Down syndrome is a genetic disorder that results in an extra copy of chromosome 21. People with mosaic Down syndrome have a mixture of cells. Some have two copies of chromosome 21, and some have three. Mosaic Down syndrome occurs in about 2 percent of all Down syndrome cases.

What causes Afibrinogenemia?

Congenital afibrinogenemia is caused by a complete absence of fibrinogen protein. Most FGA, FGB, and FGG gene mutations that cause this condition result in a premature stop signal in the instructions for making the respective protein. If any protein is made, it is nonfunctional.

What does Dysfibrinogenemia mean?

Dysfibrinogenemia is a coagulation (clotting) disorder characterized by having an abnormal form of fibrinogen.[11855] Fibrinogen is a protein produced by the liver which helps control bleeding by helping blood clots to form.[11856] Having abnormal fibrinogen results in defective clot formation and can cause an ...

What is Parahemophilia?

Factor V deficiency is also known as Owren's disease or parahemophilia. It's a rare bleeding disorder that results in poor clotting after an injury or surgery. Factor V deficiency shouldn't be confused with factor V Leiden mutation, a much more common condition that causes excessive blood clotting.

What is the ICD-10 code for coagulation defects?

286.9 is a legacy non-billable code used to specify a medical diagnosis of other and unspecified coagulation defects. This code was replaced on September 30, 2015 by its ICD-10 equivalent.

What is a code also note?

Code also note - A "code also" note instructs that two codes may be required to fully describe a condition, but this note does not provide sequencing direction.

What is the ICd 9 code for a syringe?

ICD-9-CM 286.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim , however, 286.0 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).

Is hemophilia a hereditary disorder?

A deficiency or abnormality of a blood coagulation factor characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage, hemophilia is typically a hereditary disorder but, rarely, may be acquired. Inherited coagulation factor-deficient hemophilias include hemophilia a or classic hemophilia (factor viii deficiency) hemophilia b or christmas disease (factor ix deficiency), and hemophilia c (factor xi deficiency). In individuals without hereditary hemophilia a, factor viii inhibitors may occur spontaneously as autoantibodies, resulting in a condition known as 'acquired hemophilia.' approximately 10 % of patients with acquired hemophilia have an underlying malignancy

When will the ICD-10-CM Q99.9 be released?

The 2022 edition of ICD-10-CM Q99.9 became effective on October 1, 2021.

What is chromosomal anomaly?

Chromosomal anomaly. Genetic disorder. Clinical Information. A disorder that results from a chromosomal abnormality. Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from thompson et al., genetics in medicine, 5th ed, p429) ...

What is a chromosome condition?

Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material, either a whole chromosome or a chromosome segment.

What is the ICd 10 code for factor ix?

286.1 is a legacy non-billable code used to specify a medical diagnosis of congenital factor ix disorder. This code was replaced on September 30, 2015 by its ICD-10 equivalent.

What is a code also note?

Code also note - A "code also" note instructs that two codes may be required to fully describe a condition, but this note does not provide sequencing direction.