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Q87.19 Other congenital malformation syndromes predominantly associated with short stature
BackQ87Other specified congenital malformation syndromes affecting multiple systemsCategory7 →Q87.0Congenital malformation syndromes predominantly affecting facial appearanceCategoryQ87.1Congenital malformation syndromes predominantly associated with short statureCategory2 →Q87.11Prader-Willi syndromeCategoryQ87.19Other congenital malformation syndromes predominantly associated with short statureCategoryQ87.2Congenital malformation syndromes predominantly involving limbsCategoryQ87.3Congenital malformation syndromes involving early overgrowthCategoryQ87.4Marfan syndromeCategory4 →Q87.40Marfan syndrome, unspecifiedCategoryQ87.41Marfan syndrome with cardiovascular manifestationsCategory2 →Q87.410Marfan syndrome with aortic dilationCategoryQ87.418Marfan syndrome with other cardiovascular manifestationsCategoryQ87.42Marfan syndrome with ocular manifestationsCategoryQ87.43Marfan syndrome with skeletal manifestationCategoryQ87.5Other congenital malformation syndromes with other skeletal changesCategoryQ87.8Other specified congenital malformation syndromes, not elsewhere classifiedCategory9 →Q87.81Alport syndromeCategoryQ87.82Arterial tortuosity syndromeCategoryQ87.83Bardet-Biedl syndromeCategoryQ87.84Laurence-Moon syndromeCategoryQ87.85MED13L syndromeCategoryQ87.86Kleefstra syndromeCategoryQ87.87Hao-Fountain SyndromeCategoryQ87.88CTNNB1 syndromeCategoryQ87.89Other specified congenital malformation syndromes, not elsewhere classifiedCategory
CategoryCODABLE
Q87.19
Other congenital malformation syndromes predominantly associated with short stature
EXAMPLES
Aarskog syndrome
Cockayne syndrome
De Lange syndrome
Dubowitz syndrome
Noonan syndrome
Robinow-Silverman-Smith syndrome
Russell-Silver syndrome
Seckel syndrome
Cockayne syndrome
De Lange syndrome
Dubowitz syndrome
Noonan syndrome
Robinow-Silverman-Smith syndrome
Russell-Silver syndrome
Seckel syndrome
- Chapter
- XVII · Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders
- Section
- Q80-Q89
- Valid from
Source
CMS ICD-10-CM Tabular List, edition FY2026.