 E34 |
 |
Other endocrine disorders  |
| |
| Excludes1 |
pseudohypoparathyroidism (E20.1)
|
|
| |
 E34.0 |
|
Carcinoid syndrome |
| |
| Notes |
May be used as an additional code to identify functional activity associated with a carcinoid tumor.
|
|
|
| |
| 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 |
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| 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 |
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