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ICD-10-CM Codes E00-E89 E20-E35 E34 E34.321

ICD-10-CM Diagnosis Code E34.321

Effective Date: 10/01/2022 To 09/30/2025

Primary insulin-like growth factor-1 (IGF-1) deficiency

CMS-HCC-V24	CMS-HCC-V28	RxHCC	Age	Gender	Maternity	Acute or Chronic	MCC
--	--	--	--	--	--	Acute	No

Applicable To for E34.321:

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

Back-references to E34.321

Dwarfism see also Short, stature E34.328

Laron-type see also Short, stature E34.321

Short, shortening, shortness

stature(child) (hereditary) (idiopathic) NEC R62.52
- Laron-type E34.321
- due to
  - genetic causes E34.329
    - acid-labile subunit gene(IGFALS) defect E34.321
    - growth hormone gene 1(GH1) defect with growth hormone neutralizing antibodies E34.321
    - growth hormone insensitivity syndrome(GHIS) E34.321
    - insulin-like growth factor 1 gene(IGF1) defect E34.321
    - primary insulin-like growth factor-1(IGF-1) deficiency E34.321
    - severe primary insulin-like growth factor-1 deficiency(SPIGFD) E34.321
    - signal transducer and activator of transcription 5B gene(STAT5b) defect E34.321

Chapter, Section and Diagnosis Prefix for E34.321

Endocrine, nutritional and metabolic diseases

Disorders of other endocrine glands

Other endocrine disorders