5 result found:

Congenital malformation syndromes predominantly involving limbs
ICD-10-CM Diagnosis Code Q87.2

Congenital malformation syndromes predominantly involving limbs

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Applicable To
  • Holt-Oram syndrome
  • Klippel-Trenaunay-Weber syndrome
  • Nail patella syndrome
  • Rubinstein-Taybi syndrome
  • Sirenomelia syndrome
  • Thrombocytopenia with absent radius [TAR] syndrome
  • VATER syndrome
Anonychia
nail patella syndrome (Q87.2)
ICD-10-CM Diagnosis Code Q84.3

Anonychia

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Type 1 Excludes
  • nail patella syndrome (Q87.2)
Hereditary nephropathy, not elsewhere classified
Alport's syndrome (Q87.81-); hereditary amyloid nephropathy (E85.-); nail patella syndrome (Q87.2); non-neuropathic heredofamilial amyloidosis (E85.-)
ICD-10-CM Diagnosis Code N07
  • N07 Hereditary nephropathy, not elsewhere classif...
    • N07.0 Hereditary nephropathy, not elsewhere classif...
    • N07.1 Hereditary nephropathy, not elsewhere classif...
    • N07.2 Hereditary nephropathy, not elsewhere classif...
    • N07.3 Hereditary nephropathy, not elsewhere classif...
    • N07.4 Hereditary nephropathy, not elsewhere classif...
    • N07.5 Hereditary nephropathy, not elsewhere classif...
    • N07.6 Hereditary nephropathy, not elsewhere classif...
    • N07.7 Hereditary nephropathy, not elsewhere classif...
    • N07.8 Hereditary nephropathy, not elsewhere classif...
    • N07.9 Hereditary nephropathy, not elsewhere classif...
    • N07.A Hereditary nephropathy, not elsewhere classif...
Congenital and hereditary thrombocytopenia purpura
Congenital and hereditary thrombocytopenic purpura; congential or hereditary disorder, such as:; thrombocytopenia with absent radius (TAR syndrome) (Q87.2); Congenital thrombocytopenia; Hereditary thrombocytopenia
ICD-10-CM Diagnosis Code D69.42

Congenital and hereditary thrombocytopenia purpura

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Congenital thrombocytopenia
  • Hereditary thrombocytopenia
Code First
  • congential or hereditary disorder, such as:
  • thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
Congenital malformation of knee
Bifid patella; Bipartite patella (kneecap); Congenital bilateral genu valgum; Congenital bilateral genu varum; Congenital dislocation of bilateral patella; Congenital dislocation of bilateral patellae; Congenital dislocation of left patella; Congenital dislocation of patella; Congenital dislocation of right patella; Congenital dislocation patella (kneecap); Congenital genu valgum; Congenital genu valgum of bilateral knees; Congenital genu valgum of left knee; Congenital genu valgum of right knee; Congenital genu valgum, both sides; Congenital genu varum; Congenital left genu valgum; Congenital left genu varum; Congenital right genu valgum; Congenital right genu varum; Genu valgum, congenital; Genu varum, congenital; congenital dislocation of knee (Q68.2); congenital genu recurvatum (Q68.2); nail patella syndrome (Q87.2); Congenital absence of patella; Congenital dislocation of patella; Congenital genu valgum; Congenital genu varum; Rudimentary patella
ICD-10-CM Diagnosis Code Q74.1

Congenital malformation of knee

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Applicable To
  • Congenital absence of patella
  • Congenital dislocation of patella
  • Congenital genu valgum
  • Congenital genu varum
  • Rudimentary patella
Type 1 Excludes
  • congenital dislocation of knee (Q68.2)
  • congenital genu recurvatum (Q68.2)
  • nail patella syndrome (Q87.2)