`E72.09` Other disorders of amino-acid transport

Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.

Risk adjustment (HCC)

CMS-HCC V22: HCC 23 — Other Significant Endocrine and Metabolic Disorders
RxHCC V08: HCC 43 — Pituitary, Adrenal Gland, and Other Endocrine and Metabolic Disorders
ESRD V24: HCC 23

Defines the logic of DRG(s) 642 in MDC 10.

Type 1 Excludes: E72.04 Cystinosis ("Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09)")

Type 1 Excludes: D61.03 Fanconi anemia ("Fanconi syndrome (E72.0-)")
Type 1 Excludes: N29 Other disorders of kidney and ureter in diseases classified elsewhere ("cystinosis (E72.0)")

Type 2 Excludes: G11 Hereditary ataxia ("metabolic disorders (E70-E88)")
Code First: G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")
Type 2 Excludes: G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")
Code First: H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")
Type 2 Excludes: N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")
Type 2 Excludes: N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")
Type 1 Excludes: P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")
Type 1 Excludes: R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of amino-acid metabolism (E70-E72)")
Type 1 Excludes: R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")

Beta-mercaptolactate-cysteine disulfiduria
Blue › diaper syndrome
De Toni-Fanconi (-Debré) syndrome
Disorder (of) › amino-acid › glycinuria
Disorder (of) › amino-acid › renal transport NEC
Disorder (of) › amino-acid › transport NEC
Dwarfism › nephrotic-glycosuric (with hypophosphatemic rickets)
Fanconi (-de Toni)(-Debré) syndrome
Glycinuria (renal) (with ketosis)
Lignac (-de Toni) (-Fanconi) (-Debré) disease or syndrome
Rickets (active) (acute) (adolescent) (chest wall) (congenital) (current) (infantile) (intestinal) › hypophosphatemic with nephrotic-glycosuric dwarfism
Sclerosis, sclerotic › renal › with › cystine storage disease
Stone (s) › cystine
Syndrome › de Toni-Fanconi (-Debré)
Syndrome › Fanconi (-de Toni) (-Debré)
Syndrome › Lignac (de Toni) (-Fanconi) (-Debré)
Syndrome › Toni-Fanconi
Toni-Fanconi syndrome (cystinosis)