E34.328✓ Billable
Other genetic causes of short stature
Inclusion Terms
- •Short stature due to ACAN gene variant
- •Short stature due to aggrecan deficiency
- •Short stature due to NPR-2 gene variant
Also Indexed As(ICD-10-CM Alphabetic Index)
These clinical terms, synonyms, and manifestations all map to E34.328 in the official ICD-10-CM Alphabetic Index.
Deficiency, deficient, short stature homeobox gene (SHOX), with, short stature (idiopathic)DwarfismDwarfism, congenitalDwarfism, infantileShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, ACAN gene variantShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, NPR-2 gene variantShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, aggrecan deficiencyShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, specified genetic cause NEC
Code Hierarchy
┌4Endocrine, nutritional and metabolic diseases (E00-E89)├E20-E35Disorders of other endocrine glands (E20-E35)├E34Other endocrine disorders
└E34.328Other genetic causes of short stature
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