2024 ICD-10-CM Diagnosis Code Q87.5

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

• 3-M syndrome
• Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
• Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome
• Antley-Bixler syndrome
• Arachnodactyly
• Arachnodactyly with abnormal ossification and intellectual disability syndrome
• Autosomal recessive distal osteolysis syndrome
• Baller-Gerold syndrome
• Beemer Ertbruggen syndrome
• BRESEK syndrome
• Cardiospondylocarpofacial syndrome
• CLOVE syndrome
• Combined immunodeficiency with faciooculoskeletal anomalies syndrome
• Conductive deafness, ptosis, skeletal anomalies syndrome
• Congenital abnormal fusion of humerus
• Congenital abnormal shape of clavicle
• Congenital abnormal shape of clavicle
• Congenital abnormal shape of clavicle
• Congenital anomaly of subcutaneous tissue
• Congenital anomaly of subcutaneous tissue
• Congenital anomaly of subcutaneous tissue
• Congenital atresia of external auditory canal
• Congenital atrophy of optic nerve
• Congenital bowing of femur
• Congenital bowing of long bone
• Congenital corneal leukoma
• Congenital deformity of clavicle
• Congenital deformity of clavicle
• Congenital deformity of clavicle
• Congenital deformity of shoulder
• Congenital deformity of shoulder
• Congenital deformity of shoulder
• Congenital insufficiency of mitral valve
• Congenital leg bone bowing
• Corneal leukoma
• Cutis verticis gyrata
• Dacryocystitis and osteopoikilosis syndrome
• FG syndrome
• Humeroradial synostosis
• Idiopathic osteolyses
• Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome
• Jarcho-Levin syndrome
• Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
• Mandibuloacral dysostosis
• Mandibuloacral dysostosis
• Mandibuloacral dysostosis
• Mandibuloacral dysplasia with type A lipodystrophy
• Mandibuloacral dysplasia with type B lipodystrophy
• Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome
• Multicentric carpotarsal osteolysis syndrome
• Osteopoikilosis
• Otopalatodigital syndrome spectrum disorder
• Otospondylomegaepiphyseal dysplasia
• Primary testicular failure
• Retinal pigment epithelial dystrophy
• Richieri Costa-da Silva syndrome
• Saldino-Mainzer dysplasia
• Scalp defect postaxial polydactyly syndrome
• Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome
• Spondylodysplasia
• Stenosis of lacrimal canaliculi
• Testicular hypofunction
• X-linked intellectual disability, craniofacioskeletal syndrome

Clinical Information

• Arachnodactyly

  an abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar side of the hand. arachnodactyly can include feet and toes. arachnodactyly has been associated with several gene mutations and syndromes.

• Osteopoikilosis

  an asymptomatic, autosomal dominant trait in which pea-sized sclerotic spots, prominent in the metaphyseal area, are accompanied by unique cutaneous lesions. these are yellowish papules or plaques with increased elastin content. (from cecil textbook of medicine, 19th ed, pp1434-35)

• Osteopoikilosis

  a rare autosomal dominant inherited disorder characterized by the presence of small areas of increased density throughout the bones.

Q87.5 is grouped with Diagnostic Related Groups - MS-DRG Mapping

Diagnostic Related Groups (DRGs) are a classification system used to group together diagnosis codes for the purpose of reimbursement and healthcare management. DRGs are used to standardize the way hospitals and other providers are paid for inpatient services. In this system patients are grouped together based on their principal diagnosis in areas referred to as Major Diagnostic Categories (MDC). Once a patient is assigned a particular diagnostic category, providers receive a predetermined payment rate for the services rendered. This reimbursement rate is often fixed and is meant to cover the cost of care for that patient. Reimbursement is also affected by the relative weight of a diagnostic related group based on the severity of a patient's illness and the associated cost of care during hospitalization.

Diagnostic related groups encourage healthcare providers to focus on quality and efficiency in patient care while managing costs effectively. The diagnosis code is present in the following groups for version MS-DRG V41.0 applicable from 10/01/2023 through 09/30/2024.

The relative weight of a diagnostic related group determines the reimbursement rate based on the severity of a patient's illness and the associated cost of care during hospitalization.

Present on Admission (POA)

Q87.5 is exempt from POA reporting - The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement. Review other POA exempt codes here.

CMS POA Indicator Options and Definitions

Convert Q87.5 to ICD-9-CM

• ICD-9-CM Code: 759.89 - Specfied cong anomal NEC
  Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.

Code History

• FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
• FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
• FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
• FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
• FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
• FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
• FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
• FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
• FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.