10 result found:

Congenital malformation syndromes predominantly associated with short stature
ICD-10-CM Diagnosis Code Q87.1

Congenital malformation syndromes predominantly associated with short stature

    2016 2017 2018 2019 2020 - Converted to Parent Code 2021 Non-Billable/Non-Specific Code
Type 1 Excludes
  • Ellis-van Creveld syndrome (Q77.6)
  • Smith-Lemli-Opitz syndrome (E78.72)
Prader-Willi syndrome
ICD-10-CM Diagnosis Code Q87.11

Prader-Willi syndrome

    2020 - New Code 2021 Billable/Specific Code POA Exempt
Other congenital malformation syndromes predominantly associated with short stature
ICD-10-CM Diagnosis Code Q87.19

Other congenital malformation syndromes predominantly associated with short stature

    2020 - New Code 2021 Billable/Specific Code POA Exempt
Applicable To
  • Aarskog syndrome
  • Cockayne syndrome
  • De Lange syndrome
  • Dubowitz syndrome
  • Noonan syndrome
  • Robinow-Silverman-Smith syndrome
  • Russell-Silver syndrome
  • Seckel syndrome
Epidermolysis bullosa simplex
Cockayne's syndrome (Q87.19)
ICD-10-CM Diagnosis Code Q81.0

Epidermolysis bullosa simplex

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Type 1 Excludes
Turner's syndrome
Noonan syndrome (Q87.19)
ICD-10-CM Diagnosis Code Q96
  • Q96 Turner's syndrome
    • Q96.0 Karyotype 45, X
    • Q96.1 Karyotype 46, X iso (Xq)
    • Q96.2 Karyotype 46, X with abnormal sex chromosome,...
    • Q96.3 Mosaicism, 45, X/46, XX or XY
    • Q96.4 Mosaicism, 45, X/other cell line(s) with abno...
    • Q96.8 Other variants of Turner's syndrome
    • Q96.9 Turner's syndrome, unspecified
Hypothalamic dysfunction, not elsewhere classified
Exercise induced hypothalamic insufficiency; Hypothalamic insufficiency, exercise induced; Hypothalamic insufficiency, primary; Hypothalamic syndrome; Primary hypothalamic insufficiency; Prader-Willi syndrome (Q87.11); Russell-Silver syndrome (Q87.19)
ICD-10-CM Diagnosis Code E23.3

Hypothalamic dysfunction, not elsewhere classified

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Type 1 Excludes
  • Prader-Willi syndrome (Q87.11)
  • Russell-Silver syndrome (Q87.19)
Disorders of purine and pyrimidine metabolism
Ataxia-telangiectasia (Q87.19); Bloom's syndrome (Q82.8); Cockayne's syndrome (Q87.19); calculus of kidney (N20.0); combined immunodeficiency disorders (D81.-); Fanconi's anemia (D61.09); gout (M1A.-, M10.-); orotaciduric anemia (D53.0); progeria (E34.8); Werner's syndrome (E34.8); xeroderma pigmentosum (Q82.1)
ICD-10-CM Diagnosis Code E79
  • E79 Disorders of purine and pyrimidine metabolism...
    • E79.0 Hyperuricemia without signs of inflammatory a...
    • E79.1 Lesch-Nyhan syndrome
    • E79.2 Myoadenylate deaminase deficiency
    • E79.8 Other disorders of purine and pyrimidine meta...
    • E79.9 Disorder of purine and pyrimidine metabolism,...
Cerebellar ataxia with defective DNA repair
Ataxia telangiectasia syndrome; Cockayne's syndrome (Q87.19); other disorders of purine and pyrimidine metabolism (E79.-); xeroderma pigmentosum (Q82.1); Ataxia telangiectasia [Louis-Bar]
ICD-10-CM Diagnosis Code G11.3

Cerebellar ataxia with defective DNA repair

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Ataxia telangiectasia [Louis-Bar]
Type 2 Excludes
  • Cockayne's syndrome (Q87.19)
  • other disorders of purine and pyrimidine metabolism (E79.-)
  • xeroderma pigmentosum (Q82.1)
Overweight and obesity
obesity complicating pregnancy, childbirth and the puerperium, if applicable (O99.21-); adiposogenital dystrophy (E23.6); lipomatosis NOS (E88.2); lipomatosis dolorosa [Dercum] (E88.2); Prader-Willi syndrome (Q87.11); code to identify body mass index (BMI), if known (Z68.-)
ICD-10-CM Diagnosis Code E66
  • E66 Overweight and obesity
    • E66.0 Obesity due to excess calories
      • E66.01 Morbid (severe) obesity due to excess calorie...
      • E66.09 Other obesity due to excess calories
    • E66.1 Drug-induced obesity
    • E66.2 Morbid (severe) obesity with alveolar hypoven...
    • E66.3 Overweight
    • E66.8 Other obesity
    • E66.9 Obesity, unspecified
Short stature due to endocrine disorder
Constitutional short stature; Dwarfism; Homozygous leri weill dyschondrosteosis syndrome; Langer mesomelic dysplasia syndrome; Short stature; True dwarfism; achondroplastic short stature (Q77.4); hypochondroplastic short stature (Q77.4); nutritional short stature (E45); pituitary short stature (E23.0); progeria (E34.8); renal short stature (N25.0); Russell-Silver syndrome (Q87.19); short-limbed stature with immunodeficiency (D82.2); short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index; short stature NOS (R62.52); Constitutional short stature; Laron-type short stature
ICD-10-CM Diagnosis Code E34.3

Short stature due to endocrine disorder

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Constitutional short stature
  • Laron-type short stature
Type 1 Excludes
  • achondroplastic short stature (Q77.4)
  • hypochondroplastic short stature (Q77.4)
  • nutritional short stature (E45)
  • pituitary short stature (E23.0)
  • progeria (E34.8)
  • renal short stature (N25.0)
  • Russell-Silver syndrome (Q87.19)
  • short-limbed stature with immunodeficiency (D82.2)
  • short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
  • short stature NOS (R62.52)