Q87.5
BillableOth congenital malformation syndromes w oth skeletal changes
Other congenital malformation syndromes with other skeletal changes
Status
Billable / Specific
Parent Code
Q87Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Use Additional Code
Additional codes that should follow this code
- code(s) to identify all associated manifestations
Also Known As / Clinical Terms
SNOMED CT
- Congenital deformity of clavicle7921007
- Buschke-Ollendorff syndrome9147009
- Osteopoikilosis9147009
- Congenital insufficiency of mitral valve29928006
- Congenital mitral insufficiency29928006
- Congenital mitral regurgitation29928006
- MR - Congenital mitral regurgitation29928006
- Congenital angulated femur33534005
- Congenital bent femur33534005
- Congenital bowed femur33534005
- Congenital bowing of femur33534005
- FG syndrome49984004
- Cutis verticis gyrata51603000
- Congenital anomaly of subcutaneous tissue56759000
- Autosomal recessive spondylocostal dysostosis61367005
- Jarcho-Levin syndrome61367005
- Spondylothoracic dysplasia61367005
- Arachnodactyly62250003
- Congenital arachnodactyly62250003
- Spider finger62250003
- Antley-Bixler syndrome62964007
- Multisynostotic osteodysgenesis62964007
- Trapezoidcephaly-multiple synostosis62964007
- Atresia of external auditory canal75355004
- Congenital atresia of external auditory canal75355004
- Baller-Gerold syndrome77608001
- Craniosynostosis-radial aplasia syndrome77608001
- Stenosis of lacrimal canaliculi81345003
- Stenosis of lacrimal canaliculus81345003
- Stenosis of lacrimal passage81345003
- Congenital abnormal fusion of humerus92859003
- Congenital fused humerus92859003
- Congenital abnormal shape of clavicle92906004
- Congenital misshapen clavicle92906004
- Lambdoid craniosynostosis109417006
- Parieto-occipital craniosynostosis109417006
- Craniomandibular dermatodysostosis109419009
- Familial mandibuloacral dysplasia109419009
- Mandibuloacral dysostosis109419009
- Mandibuloacral dysplasia109419009
- Humeroradial synostosis205329008
- Spondylodysplasia254045003
- Otospondylomegaepiphyseal dysplasia254060000
- Conorenal syndrome254092004
- Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome254092004
- Saldino-Mainzer dysplasia254092004
- Idiopathic osteolyses254147009
- Primary failure of the testes370997001
- Primary testicular failure370997001
- Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma403766000
- Rosenthal-Klöpfer syndrome403766000
- 3-M syndrome702342007
- 3M syndrome702342007
- Dolichospondylic dysplasia702342007
- Le Merrer syndrome702342007
- Miller-McKusick-Malvaux syndrome702342007
- Corneal leucoma704272003
- Corneal leukoma704272003
- Autosomal recessive distal osteolysis syndrome715487005
- Distal osteolysis, short stature and intellectual disability715487005
- Petit Fryns syndrome715487005
- Beemer Ertbruggen syndrome717859007
- Beemer lethal malformation syndrome717859007
- Hydrocephalus, cardiac malformation, dense bone syndrome717859007
- BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome717945001
- BRESEK syndrome717945001
- Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome717945001
- Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome717945001
- X-linked mental retardation Reish type717945001
- CLOVE syndrome719475006
- CLOVES syndrome719475006
- Congenital lipomatous overgrowth, vascular malformation, epidermal naevi, skeletal anomaly syndrome719475006
- Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome719475006
- Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome720495005
- Cassia Stocco dos Santos syndrome720495005
- Arachnodactyly with abnormal ossification and intellectual disability syndrome720501007
- Kosztolanyi syndrome720501007
- Cardiospondylocarpofacial syndrome720612000
- Forney Robinson Pascoe syndrome720612000
- Forney syndrome720612000
- Mitral regurgitation with deafness and skeletal anomalies syndrome720612000
- Dacryocystitis and osteopoikilosis syndrome721082002
- Gunal Seber Basaran syndrome721082002
- Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome722459008
- Sohval Soffer syndrome722459008
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- Scalp defect postaxial polydactyly syndrome726629006
- Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome733419006
- Conductive deafness, ptosis, skeletal anomalies syndrome763213001
- Jackson Barr syndrome763213001
- Multicentric carpotarsal osteolysis syndrome766992008
- Combined immunodeficiency with faciooculoskeletal anomalies syndrome770625006
- Roifman Chitayat syndrome770625006
- Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency770755007
- Congenital disorder of glycosylation due to PIGT deficiency770755007
- Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome770755007
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3770755007
- X-linked intellectual disability, craniofacioskeletal syndrome773274001
- SAMS (short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies) syndrome774155009
- SAMS syndrome774155009
- Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome774155009
- Myotonia, intellectual disability, skeletal anomalies syndrome782941005
- Richieri Costa-da Silva syndrome782941005
- OPD (otopalatodigital) spectrum disorder784010006
- Otopalatodigital syndrome spectrum disorder784010006
- Mandibuloacral dysostosis co-occurrent with type A lipodystrophy1003431005
- Mandibuloacral dysplasia with type A lipodystrophy1003431005
- Mandibuloacral dysostosis co-occurrent with type B lipodystrophy1003432003
- Mandibuloacral dysplasia with type B lipodystrophy1003432003
- Congenital dysplasia of radius1142185008
- Congenital corneal leucoma1217688006
- Congenital corneal leukoma1217688006
- Congenital deformity of shoulder1230384009
- Retinal pigment epithelial dystrophy342581000119102
Frequently Asked Questions
What is the ICD-10 code for oth congenital malformation syndromes w oth skeletal changes?
The ICD-10-CM code for oth congenital malformation syndromes w oth skeletal changes is Q87.5. The full clinical description is "Other congenital malformation syndromes with other skeletal changes". Q87.5 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q87.5 mean?
ICD-10-CM code Q87.5 represents "Other congenital malformation syndromes with other skeletal changes". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q87.5 a billable code?
Yes, Q87.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q87.5 in?
Q87.5 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
Are additional codes required with Q87.5?
Yes, when using Q87.5 you should also code: code(s) to identify all associated manifestations.
What SNOMED CT codes does Q87.5 map to?
Q87.5 maps to 52 SNOMED CT concepts: 702342007, 403766000, 720495005, 62964007, 62250003, and 47 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q87.5?
Q87.5 is linked to 1 UMLS Concept Unique Identifier: C0478093. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.