icd 10 code for alport syndrome

What is Alport disease?

Alport syndrome is a disease that damages the tiny blood vessels in your kidneys. It can lead to kidney disease and kidney failure. It can also cause hearing loss and problems within the eyes. Alport syndrome causes damage to your kidneys by attacking the glomeruli.

What causes Alport syndrome?

Causes. Mutations in the COL4A3, COL4A4, and COL4A5 genes cause Alport syndrome. These genes each provide instructions for making one component of a protein called type IV collagen. This protein plays an important role in the kidneys , specifically in structures called glomeruli.

What is other specified congenital malformation syndromes?

89 for Other specified congenital malformation syndromes, not elsewhere classified is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

Is an ICD-10 code a diagnosis?

Used for medical claim reporting in all healthcare settings, ICD-10-CM is a standardized classification system of diagnosis codes that represent conditions and diseases, related health problems, abnormal findings, signs and symptoms, injuries, external causes of injuries and diseases, and social circumstances.May 20, 2021

Why is Alport syndrome nephritic?

Alport syndrome is a nephritic syndrome caused by a mutation in the COL4A3, COL4A4, and COL4A5 genes that encode the alpha-5 chain of type IV collagen and results in altered type IV collagen strands.

Who is affected by Alport syndrome?

Alport syndrome is estimated to account for 3% of children with chronic kidney disease and 0.2% of adults with end-stage renal disease in the United States. In XLAS, males are affected more severely than females. In the autosomal forms of Alport syndrome, males and females are affected with equal severity.

What is ICD-10 code for vacterl syndrome?

EntryH01195 DiseaseOther DBsICD-11: LD2F.11 ICD-10: Q87.2 MeSH: C564752 OMIM: 276950 192350 314390 619227ReferencePMID:20849991AuthorsSchramm C, Draaken M, Bartels E, Boemers TM, Aretz S, Brockschmidt FF, Nothen MM, Ludwig M, Reutter HTitleDe novo microduplication at 22q11.21 in a patient with VACTERL association.33 more rows

What is the ICD-10 code for Loeys Dietz syndrome?

EntryH00800 DiseaseOther DBsICD-11: LD28.01 ICD-10: I71.0 MeSH: D055947 OMIM: 609192 608967 610168 610380 613795 614816 615582ReferencePMID:21785848AuthorsKalra VB, Gilbert JW, Malhotra ATitleLoeys-Dietz syndrome: cardiovascular, neuroradiological and musculoskeletal imaging findings.29 more rows

What is the ICD-10 code for Bardet Biedl?

Bardet-Biedl Syndrome D020788.

Is ICD-10 covered by Medicare?

The ICD-10 transition is a mandate that applies to all parties covered by HIPAA, not just providers who bill Medicare or Medicaid.

WHO ICD-10 classification?

ICD-10 is the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD), a medical classification list by the World Health Organization (WHO).

How do I find my diagnosis code?

If you need to look up the ICD code for a particular diagnosis or confirm what an ICD code stands for, visit the Centers for Disease Control and Prevention (CDC) website to use their searchable database of the current ICD-10 codes.Jan 9, 2022

The ICD code Q878 is used to code Neu-Laxova syndrome

Neu-laxova syndrome (also known as neu syndrome or neu-povysilová syndrome, abbreviated as nls) is a rare autosomal recessive disorder characterized by severe intrauterine growth restriction and multiple congenital malformations. Neu-laxova syndrome is a very severe disorder, leading to stillbirth or neonatal death. it was first described by dr.

Coding Notes for Q87.81 Info for medical coders on how to properly use this ICD-10 code

Use Additional Code note means a second code must be used in conjunction with this code. Codes with this note are Etiology codes and must be followed by a Manifestation code or codes.

MS-DRG Mapping

DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with MCC.

ICD-10-CM Alphabetical Index References for 'Q87.81 - Alport syndrome'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q87.81. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code Q87.81 and a single ICD9 code, 759.89 is an approximate match for comparison and conversion purposes.

What does "use additional code" mean?

The “use additional code” indicates that a secondary code could be used to further specify the patient’s condition. This note is not mandatory and is only used if enough information is available to assign an additional code.

What is the tabular list of diseases and injuries?

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code Q87.81:

How many babies are born with birth defects?

Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect. A birth defect may affect how the body looks, works or both. Some birth defects like cleft lip or neural tube defects are structural problems that can be easy to see.

Can birth defects be diagnosed during pregnancy?

For most birth defects, the cause is unknown. Health care providers can diagnose certain birth defects during pregnancy, with prenatal tests. That's why it important to get regular prenatal care. Other birth defects may not be found until after the baby is born.

What is the most common form of nephritis?

a group of inherited conditions characterized initially by hematuria and slowly progressing to renal insufficiency. the most common form is the alport syndrome hereditary nephritis with hearing loss which is caused by mutations in genes for type iv collagen and defective glomerular basement membrane.

What is the GEM crosswalk?

The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code Q87.81 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.

What does it mean when you have blood in your urine?

Almost all affected individuals have blood in their urine (hematuria), which indicates abnormal functioning of the kidneys. Many people with Alport syndrome also develop high levels of protein in their urine (proteinuria).