icd 10 code for chromosone partial deletion

What is the ICD 10 code for chromosome deletion?

Q93.5 is a billable ICD code used to specify a diagnosis of other deletions of part of a chromosome. A 'billable code' is detailed enough to be used to specify a medical diagnosis. Documentation insufficient to determine if the condition was present at the time of inpatient admission.

What is the ICD 10 code for partial trisomy and autosome?

2019 ICD-10-CM Diagnosis Code Q92.9 Trisomy and partial trisomy of autosomes, unspecified Billable/Specific Code POA Exempt The following code (s) above Q92.9 contain annotation back-references that may be applicable to Q92.9 : Approximate Synonyms Present On Admission Q92.9 is considered exempt from POA reporting.

What is deletion of the short arm of chromosome 5?

Deletion of short arm of chromosome 5. An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, mental retardation, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-).

What is Z15 89?

ICD-10 code Z15. 89 for Genetic susceptibility to other disease is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .

What does the deletion of an entire Autosome cause?

Abstract. Most cytologically visible autosomal deletions cause multiple malformations and mental retardation. A small proportion of deletions produce recognizable phenotypes, these are called segmental aneusomy or contiguous gene syndromes.

What is the ICD-10-CM code for Digeorge syndrome?

D82. 1 - Di George's syndrome | ICD-10-CM.

What is the ICD-10 code for developmental delay?

315.9 - Unspecified delay in development | ICD-10-CM.

What are the two types of chromosome deletions that can occur?

Types of deletion include the following: Terminal deletion – a deletion that occurs towards the end of a chromosome. Intercalary/interstitial deletion – a deletion that occurs from the interior of a chromosome.

What is a chromosome deletion?

A deletion, as related to genomics, is a type of mutation that involves the loss of one or more nucleotides from a segment of DNA. A deletion can involve the loss of any number of nucleotides, from a single nucleotide to an entire piece of a chromosome.

Is DiGeorge syndrome genetic?

DiGeorge syndrome is caused by a problem with a person's genes, called 22q11 deletion. It is not usually passed on to a child by their parents, but it is in a few cases. It's often diagnosed soon after birth with a blood test to check for the genetic fault.

What is the ICD-10 CM code for Wiskott Aldrich syndrome?

D82. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the ICD-10 code for tetralogy of Fallot?

3: Tetralogy of Fallot.

What is ICD-10 code F88?

ICD-10 code: F88 Other disorders of psychological development.

How do you code developmental delays?

ICD-9-CM Diagnosis Code 315.9 : Unspecified delay in development.

What are the four types of developmental disabilities?

There are four main types of developmental disorders: nervous system disabilities, sensory related disabilities, metabolic disabilities and degenerative disorders. Many different subsets of disabilities nest under these four main groups.

What is the ICd 10 code for deletion of chromosomes?

Other deletions of part of a chromosome 1 Q93.5 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail. 2 The 2021 edition of ICD-10-CM Q93.5 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of Q93.5 - other international versions of ICD-10 Q93.5 may differ.

What are the disorders of the long arm of chromosome 15?

A genetic syndrome characterized by mental retardation, speech impairment, microcephaly, ataxia, and seizures. The majority of cases result from deletions on the long arm of chromosome 15.

The ICD code Q935 is used to code 9q34 deletion syndrome

9q34 deletion syndrome, also known as kleefstra syndrome, is a rare genetic disorder. terminal deletions of chromosome 9q34 have been associated with childhood hypotonia, a distinctive facial appearance and developmental disability.

Coding Notes for Q93.5 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.

ICD-10-CM Alphabetical Index References for 'Q93.5 - Other deletions of part of a chromosome'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q93.5. 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 Q93.5 and a single ICD9 code, 758.39 is an approximate match for comparison and conversion purposes.