Q87.5 OTH CONGENITAL MALFORMATION SYNDROMES W OTH SKELETAL CHANGES

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 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
• 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
• 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 V42.0

1. Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
2. Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
3. Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

Crosswalk Information

ICD-10 Code		ICD-9 Code	ICD-9 Description
Q87.5		759.89	Specfied cong anomal NEC

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