|  E34 |  | Other endocrine disorders   | 
	
		|  |  | 
	
		| Excludes1 | pseudohypoparathyroidism (E20.1) 
 |  | 
|  |  | 
	
		|  E34.0 |  | Carcinoid syndrome |  
		|  |  | 
	
		| CodeAlso | the underlying disorder, such as: primary neuroendocrine tumors (C7A.-)
 secondary neuroendocrine tumors (C7B.-)
 
 |  |  |  |  | 
	
		|  E34.00 |  | Carcinoid syndrome, unspecified |  
		|  |  | 
| Carcinoid disease, unspecified |  |  |  |  |  | 
	
		|  E34.01 |  | Carcinoid heart syndrome |  
		|  |  | 
| Carcinoid heart disease |  | Hedinger syndrome |  |  |  |  |  | 
	
		|  E34.09 |  | Other carcinoid syndrome |  
		|  |  | 
| Carcinoid disease NEC |  | Carcinoid syndrome NEC |  | Other carcinoid disease |  |  |  | 
|  |  | 
	
		|  E34.1 |  | Other hypersecretion of intestinal hormones |  | 
|  |  | 
	
		|  E34.2 |  | Ectopic hormone secretion, not elsewhere classified |  
		|  |  | 
	
		| Excludes1 | ectopic ACTH syndrome (E24.3) 
 |  |  | 
|  |  | 
	
		|  E34.3 |  | Short stature due to endocrine disorder |  
		|  |  | 
	
		| Excludes1 | achondroplastic short stature (Q77.4) hypochondroplastic short stature (Q77.4)
 nutritional short stature (E45)
 pituitary short stature (E23.0)
 progeria (E34.8)
 renal short stature (N25.0)
 Russell-Silver syndrome (Q87.19)
 short-limbed stature with immunodeficiency (D82.2)
 short stature (child) (R62.52)
 short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
 short stature NOS (R62.52)
 
 |  |  |  |  | 
	
		|  E34.30 |  | Short stature due to endocrine disorder, unspecified |  |  |  |  | 
	
		|  E34.31 |  | Constitutional short stature |  
		|  |  | 
| Constitutional delay of growth, puberty, or maturation |  |  |  |  |  | 
	
		|  E34.32 |  | Genetic causes of short stature |  |  |  | 
	
		|  E34.321 |  | Primary insulin-like growth factor-1 (IGF-1) deficiency |  
		|  |  | 
| 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 |  |  |  |  |  | 
	
		|  E34.322 |  | Insulin-like growth factor-1 (IGF-1) resistance |  
		|  |  | 
| 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 |  |  |  |  |  | 
	
		|  E34.328 |  | Other genetic causes of short stature |  
		|  |  | 
| Short stature due to ACAN gene variant |  | Short stature due to aggrecan deficiency |  | Short stature due to NPR-2 gene variant |  |  |  |  |  | 
	
		|  E34.329 |  | Unspecified genetic causes of short stature |  |  |  |  |  | 
	
		|  E34.39 |  | Other short stature due to endocrine disorder |  |  | 
|  |  | 
	
		|  E34.4 |  | Constitutional tall stature |  
		|  |  |  |  | 
|  |  | 
	
		|  E34.5 |  | Androgen insensitivity syndrome |  |  |  | 
	
		|  E34.50 |  | Androgen insensitivity syndrome, unspecified |  
		|  |  | 
| Androgen insensitivity NOS |  |  |  |  |  | 
	
		|  E34.51 |  | Complete androgen insensitivity syndrome |  
		|  |  | 
| Complete androgen insensitivity |  | de Quervain syndrome |  | Goldberg-Maxwell syndrome |  |  |  |  |  | 
	
		|  E34.52 |  | Partial androgen insensitivity syndrome |  
		|  |  | 
| Partial androgen insensitivity |  | Reifenstein syndrome |  |  |  | 
|  |  | 
	
		|  E34.8 |  | Other specified endocrine disorders |  
		|  |  | 
| Pineal gland dysfunction |  | Progeria |  
		| Excludes2 | pseudohypoparathyroidism (E20.1) 
 |  |  | 
|  |  | 
	
		|  E34.9 |  | Endocrine disorder, unspecified |  
		|  |  | 
| Endocrine disturbance NOS |  | Hormone disturbance NOS |  |  |