Familial mandibuloacral dysplasia
Autosomal recessive distal osteolysis syndrome
Conorenal syndrome
Multisynostotic osteodysgenesis
Spondylodysplasia
CLOVES syndrome
Corneal leucoma
Congenital abnormal fusion of humerus
Arachnodactyly
Beemer lethal malformation syndrome
Congenital atresia of external auditory canal
Congenital bowed femur
Congenital lipomatous overgrowth, vascular malformation, epidermal naevi, skeletal anomaly syndrome
Congenital atrophy of optic nerve
Sohval Soffer syndrome
Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome
Saldino-Mainzer dysplasia
Primary failure of the testes
Corneal leukoma
Autosomal recessive spondylocostal dysostosis
Multicentric carpotarsal osteolysis syndrome
Congenital corneal leukoma
Combined immunodeficiency with faciooculoskeletal anomalies syndrome
Spider finger
Roifman Chitayat syndrome
Trapezoidcephaly-multiple synostosis
Distal osteolysis, short stature and intellectual disability
Mandibuloacral dysostosis co-occurrent with type A lipodystrophy
Antley-Bixler syndrome
Idiopathic osteolyses
Stenosis of lacrimal canaliculi
Congenital mitral insufficiency
Otopalatodigital syndrome spectrum disorder
Cardiospondylocarpofacial syndrome
Parieto-occipital craniosynostosis
Rosenthal-Klöpfer syndrome
Osteopoikilosis
3-M syndrome
Congenital mitral regurgitation
FG syndrome
MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3
Forney Robinson Pascoe syndrome
Congenital dysplasia of radius
Mandibuloacral dysostosis
CLOVE syndrome
Petit Fryns syndrome
Congenital arachnodactyly
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome
Forney syndrome
Congenital misshapen clavicle
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Buschke-Ollendorff syndrome
BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome
Congenital fused humerus
Congenital deformity of shoulder
Jackson Barr syndrome
Scalp defect postaxial polydactyly syndrome
Mitral regurgitation with deafness and skeletal anomalies syndrome
Hydrocephalus, cardiac malformation, dense bone syndrome
Mandibuloacral dysostosis co-occurrent with type B lipodystrophy
Humeroradial synostosis
Arachnodactyly with abnormal ossification and intellectual disability syndrome
MR - Congenital mitral regurgitation
Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome
Spondylothoracic dysplasia
Cassia Stocco dos Santos syndrome
Mandibuloacral dysplasia with type B lipodystrophy
Cutis verticis gyrata
Lambdoid craniosynostosis
Congenital abnormal shape of clavicle
Conductive deafness, ptosis, skeletal anomalies syndrome
Congenital anomaly of subcutaneous tissue
X-linked mental retardation Reish type
SAMS syndrome
Congenital angulated femur
Beemer Ertbruggen syndrome
Myotonia, intellectual disability, skeletal anomalies syndrome
Atresia of external auditory canal
BRESEK syndrome
Congenital optic atrophy
Retinal pigment epithelial dystrophy
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome
Primary testicular failure
Congenital bowing of femur
Craniomandibular dermatodysostosis
Baller-Gerold syndrome
Congenital deformity of clavicle
Congenital insufficiency of mitral valve
Jarcho-Levin syndrome
Congenital bent femur
X-linked intellectual disability, craniofacioskeletal syndrome
Miller-McKusick-Malvaux syndrome
OPD (otopalatodigital) spectrum disorder
Gunal Seber Basaran syndrome
Congenital disorder of glycosylation due to PIGT deficiency
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome
SAMS (short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies) syndrome
Richieri Costa-da Silva syndrome
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
Dacryocystitis and osteopoikilosis syndrome
Kosztolanyi syndrome
Congenital corneal leucoma
Craniosynostosis-radial aplasia syndrome
Mandibuloacral dysplasia
Stenosis of lacrimal passage
Otospondylomegaepiphyseal dysplasia
Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency
Dolichospondylic dysplasia
Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
Stenosis of lacrimal canaliculus
3M syndrome
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome
Le Merrer syndrome
Mandibuloacral dysplasia with type A lipodystrophy

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, also report: 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.

How does Q87.5 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth congenital malformation syndromes w oth skeletal changes affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q87.5?

Q87.5 maps to the ICD-11 code: LB9Z (Structural developmental anomalies of the skeleton, unspecified).

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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.