Other genetic causes of short stature
Billable / specific
E34.328 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Short stature due to ACAN gene variant
- Short stature due to aggrecan deficiency
- Short stature due to NPR-2 gene variant
Includes (from E34)
- Note: All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Excludes1
Not coded here — never report together with this code.
- achondroplastic short stature (Q77.4) (from E34.3)
- hypochondroplastic short stature (Q77.4) (from E34.3)
- nutritional short stature (E45) (from E34.3)
- pituitary short stature (E23.0) (from E34.3)
- progeria (E34.8) (from E34.3)
- renal short stature (N25.0) (from E34.3)
- Russell-Silver syndrome (Q87.19) (from E34.3)
- short-limbed stature with immunodeficiency (D82.2) (from E34.3)
- short stature (child) (R62.52) (from E34.3)
- short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index (from E34.3)
- short stature NOS (R62.52) (from E34.3)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E34)
- galactorrhea (N64.3) (from E34)
- gynecomastia (N62) (from E34)
- pseudohypoparathyroidism (E20.1) (from E34)
Also known as
- Short stature due to ACAN gene variant
- Short stature due to aggrecan deficiency
- Short stature due to NPR-2 gene variant
- Deficiency, deficient, short stature homeobox gene, with short stature
- Dwarfism
- Dwarfism, congenital
- Dwarfism, infantile
Parent code
- E34.32Genetic causes of short statureHeader