ICD-10-CM Diagnosis Code (2025)
Official Description for E34.32
Genetic causes of short stature
Coding Notes & Guidelines for E34.32
Inclusion Terms
- Acid-labile subunit gene (IGFALS) defect
- Growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodies
- Growth hormone insensitivity syndrome (GHIS)
- Insulin-like growth factor 1 gene (IGF1) defect
- Laron type short stature
- Severe primary insulin-like growth factor-1 deficiency (SPIGFD)
- Signal transducer and activator of transcription 5B gene (STAT5b) defect
Inclusion Terms
- Genetic syndrome with resistance to insulin-like growth factor-1
- Insulin-like growth factor-1 receptor (IGF-1R) defect
- Post-insulin-like growth factor-1 receptor signaling defect
Inclusion Terms
- Short stature due to ACAN gene variant
- Short stature due to aggrecan deficiency
- Short stature due to NPR-2 gene variant
Parent Code (Less Specific):
About ICD-10-CM Code E34.32 (Genetic causes of short stature)
ICD-10-CM code E34.32 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM E34.32 became effective on October 1, 2024.
This page provides detailed information about E34.32 - Genetic causes of short stature. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Genetic causes of short stature.