Diagnosis Code: Q87.5

Short Description: Oth congenital malformation syndromes w oth skeletal changes

Long Description: Other congenital malformation syndromes with other skeletal changes

The code Q87.5 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Oth congenital malform syndromes affecting multiple systems (Q87)
      • Q87.5 Oth congenital malformation syndromes w oth skeletal changes

Code Version: 2022 ICD-10-CM

Synonyms

• 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

Diagnostic Related Group(s)

The code Q87.5 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
• Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
• Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

« Previous Code