Diagnosis Code: Q87.2

Short Description: Congenital malformation syndromes predom involving limbs

Long Description: Congenital malformation syndromes predominantly involving limbs

The code Q87.2 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)
      • Q87.2 Congenital malformation syndromes predom involving limbs

Code Version: 2022 ICD-10-CM

Synonyms

• 4q partial monosomy syndrome
• 4q25 proximal deletion syndrome
• Aase syndrome
• Acrocardiofacial syndrome
• Acrocephalopolysyndactyly
• Acrocephalopolysyndactyly type III
• Acrocephalopolysyndactyly type IV
• Acrocephalosyndactyly
• Acrocephalosyndactyly type V
• Acrocephalosyndactyly type V
• Acrocephalosyndactyly type V
• Acrocephalosyndactyly type V
• Acrofrontofacionasal dysostosis type 2
• Acropectoral syndrome
• Acrorenal syndrome
• Acrorenoocular syndrome
• Adams-Oliver syndrome
• ADULT syndrome
• Amegakaryocytic thrombocytopenia
• Anal atresia
• Antecubital pterygium syndrome
• Ballard syndrome
• Banki syndrome
• Bent bone dysplasia group
• Bilateral hearing loss
• Brachydactyly of hand
• Brachydactyly of toes
• Brachymesophalangia
• Campomelia Cumming type
• Camptodactyly and tall stature with scoliosis and hearing loss syndrome
• Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome
• Capra DeMarco syndrome
• Catel Manzke syndrome
• Caudal appendage deafness syndrome
• Chiari malformation
• Chiari malformation type I
• Child syndrome
• Conductive hearing loss of left ear
• Conductive hearing loss of right ear
• Conductive hearing loss, bilateral
• Congenital abnormal shape of fibula
• Congenital abnormal shape of tibia
• Congenital absence of radius
• Congenital anomaly of caudal vertebra
• Congenital anomaly of patella
• Congenital cleft hand
• Congenital complete absence of bilateral lower limbs
• Congenital complete absence of bilateral upper limbs
• Congenital complete absence of left lower limb
• Congenital complete absence of left upper limb
• Congenital complete absence of lower limb
• Congenital complete absence of right lower limb
• Congenital complete absence of right upper limb
• Congenital complete absence of upper limb
• Congenital hypoplasia of femur
• Congenital hypoplastic anemia
• Congenital malposition of testis
• Congenital microgastria
• Congenital microgastria with limb reduction defect syndrome
• Congenital mixed conductive and sensorineural hearing loss
• Constitutional aplastic anemia
• Constriction ring syndrome
• Cooks syndrome
• Cryptomicrotia brachydactyly syndrome
• Curry Jones syndrome
• Deletion of part of chromosome 4
• Disorder characterized by multiple exostoses
• Duplication of fibula
• Duplication of lower limb bone
• Dystopia canthorum
• Escobar syndrome
• Femoral hypoplasia - unusual facies syndrome
• Fetal sirenomelia
• Fibular dimelia diplopodia syndrome
• Fuhrmann syndrome
• Grebe syndrome
• Guttmacher syndrome
• Hand-foot-genital syndrome
• Holt-Oram syndrome
• Hypoplasia of thumb
• Hypoplastic anemia
• Jackson-Weiss syndrome
• Karsch Neugebauer syndrome
• Langer-Giedion syndrome
• Left conductive hearing loss
• Levy-Hollister syndrome
• Limb body wall complex
• Limb reduction-ichthyosis syndrome
• Long thumb brachydactyly syndrome
• Mietens syndrome
• Mirror polydactyly, vertebral segmentation and limb defect syndrome
• Mixed conductive AND sensorineural hearing loss
• Mixed conductive and sensorineural hearing loss of left ear
• Mixed conductive and sensorineural hearing loss of right ear
• Mixed conductive and sensorineural hearing loss, bilateral
• Multiple malformation syndrome with facial-limb defects as major feature
• Multiple malformation syndrome with limb defect as major feature
• Multiple malformation syndrome, small stature, without skeletal dysplasia
• Multiple malformation syndrome, small stature, without skeletal dysplasia
• Nager syndrome
• Nail-patella syndrome
• Nievergelt's syndrome
• Oculootoradial syndrome
• Patella dysplasia
• PDE4D haploinsufficiency syndrome
• Pelviscapular dysplasia
• Pfeiffer syndrome type 1
• Pfeiffer syndrome type 2
• Pfeiffer syndrome type 3
• PHAVER syndrome
• Port-wine stain in Rubinstein-Taybi syndrome
• Proximal deletion of long arm of chromosome 4
• Radial aplasia-thrombocytopenia syndrome
• RAPADILINO syndrome
• Rubinstein-Taybi syndrome
• Rubinstein-Taybi syndrome
• Ruvalcaba syndrome
• Saethre-Chotzen syndrome
• Sensorineural hearing loss of bilateral ears
• Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome
• Short rib dysplasia
• Sirenomelus
• Split foot
• Spondylocamptodactyly syndrome
• STAR syndrome
• Summitt syndrome
• Tel Hashomer camptodactyly syndrome
• Telecanthus
• Temple Baraitser syndrome
• Temtamy preaxial brachydactyly syndrome
• Tetraamelia with multiple malformation syndrome
• Thoracomelic dysplasia
• Townes syndrome
• Trichorhinophalangeal dysplasia type I
• Trichorhinophalangeal dysplasia type III
• Trichorhinophalangeal syndrome
• Trichorhinophalangeal syndrome
• Trichorhinophalangeal syndrome
• Trichorhinophalangeal syndrome
• Trichorhinophalangeal syndrome type 1 and 3
• Undescended testicle
• VATER association
• Waardenburg syndrome
• Waardenburg syndrome type 3
• WT limb blood syndrome
• X-linked intellectual disability Stevenson type

Diagnostic Related Group(s)

The code Q87.2 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)

References to Index of Diseases and Injuries

The code Q87.2 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Holt-Oram syndrome
  • Klippel-Trenaunay-Weber syndrome
  • Nail patella syndrome
  • Rubinstein-Taybi syndrome
  • Sirenomelia syndrome
  • Thrombocytopenia with absent radius [TAR] syndrome
  • VATER syndrome

Crosswalk Information

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

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