2021 ICD-10-CM Code Q87.2

Tabular List of Diseases and Injuries

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code Q87.2:

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

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code Q87.2 are found in the index:

• - Fong's syndrome (hereditary osteo-onychodysplasia) - Q87.2

• - Holt-Oram syndrome - Q87.2

• - Klippel-Trenaunay (-Weber) syndrome - Q87.2

• - Mietens' syndrome - Q87.2

• - Nail - See Also: condition;
  • - patella syndrome - Q87.2

• - Onycho-osteodysplasia - Q87.2

• - Osteo-onycho-arthro-dysplasia - Q87.2

• - Osteo-onychodysplasia, hereditary - Q87.2

• - Österreicher-Turner syndrome - Q87.2

• - Rubinstein-Taybi syndrome - Q87.2

• - Sirenomelia (syndrome) - Q87.2

• - Syndrome - See Also: Disease;
  • - Fong's - Q87.2
  • - nail patella - Q87.2
  • - Osterreicher-Turner - Q87.2
  • - sirenomelia - Q87.2
  • - TAR (thrombocytopenia with absent radius) - Q87.2
  • - thrombocytopenia with absent radius (TAR) - Q87.2
  • - VATER - Q87.2

• - TAR (thrombocytopenia with absent radius) syndrome - Q87.2

• - Taybi's syndrome - Q87.2

• - Thrombocytopenia, thrombocytopenic - D69.6
  • - with absent radius (TAR) - Q87.2

• - Turner-Kieser syndrome - Q87.2

• - VATER syndrome - Q87.2

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

• Aase syndrome
• Acrofrontofacionasal dysostosis type 2
• Acropectoral syndrome
• Acrorenal syndrome
• Acrorenoocular syndrome
• Adams-Oliver syndrome
• ADULT syndrome
• Amegakaryocytic thrombocytopenia
• Amelia
• Antecubital pterygium syndrome
• Ballard syndrome
• Banki syndrome
• Bent bone dysplasia group
• Brachydactyly of hand
• 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
• Carpenter Waziri syndrome
• Catel Manzke syndrome
• Caudal appendage deafness syndrome
• Chiari malformation
• Chiari malformation type I
• Child syndrome
• Congenital absence of left lower limb
• Congenital absence of lower limb
• Congenital absence of right lower limb
• Congenital anomaly of caudal vertebra
• Congenital complete absence of upper limb
• Congenital hypoplasia of femur
• Congenital malformation syndromes involving limbs
• Congenital malposition of testis
• Congenital microgastria
• Congenital microgastria with limb reduction defect syndrome
• Constitutional aplastic anemia
• Constriction ring syndrome
• Cooks syndrome
• Cryptomicrotia brachydactyly syndrome
• Curry Jones syndrome
• Disorder characterized by multiple exostoses
• Duplication of fibula
• Duplication of lower limb bone
• Escobar syndrome
• Femoral hypoplasia - unusual facies syndrome
• Fibular dimelia diplopodia syndrome
• Fuhrmann syndrome
• Grebe syndrome
• Guttmacher syndrome
• Holt-Oram syndrome
• Hypoplasia of thumb
• Karsch Neugebauer syndrome
• Klein-Waardenberg's syndrome
• Langer-Giedion syndrome
• 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
• 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
• Nager syndrome
• Nail-patella syndrome
• Nievergelt's syndrome
• Oculootoradial syndrome
• Patella dysplasia
• Pelviscapular dysplasia
• PHAVER syndrome
• Port-wine stain in Rubinstein-Taybi syndrome
• Radial aplasia-thrombocytopenia syndrome
• RAPADILINO syndrome
• Rubinstein-Taybi syndrome
• Ruvalcaba syndrome
• Short rib dysplasia
• Sirenomelus
• Split foot
• Spondylocamptodactyly syndrome
• Tel Hashomer camptodactyly syndrome
• 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 type 1 and 3
• Undescended testicle
• VATER association
• WT limb blood syndrome