| ICD-10-CM-2023 > E00-E89 > E20-E35 > E34 |
E20-E35 | Disorders of other endocrine glands | |
Excl1.: | galactorrhea (N64.3) gynecomastia (N62) | |
E34 | Other endocrine disorders | |
Excl1.: | pseudohypoparathyroidism (E20.1) | |
E34.0 | Carcinoid syndrome | |
Info: | 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 | |
Excl1.: | ectopic ACTH syndrome (E24.3) | |
E34.3 | Short stature due to endocrine disorder | |
Excl1.: | 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 | |
Info: | 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 | |
Info: | 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 | |
Info: | 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 | |
Info: | 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 | |
Info: | Constitutional gigantism | |
E34.5 | Androgen insensitivity syndrome | |
E34.50 | Androgen insensitivity syndrome, unspecified | |
Info: | Androgen insensitivity NOS | |
E34.51 | Complete androgen insensitivity syndrome | |
Info: | Complete androgen insensitivity de Quervain syndrome Goldberg-Maxwell syndrome | |
E34.52 | Partial androgen insensitivity syndrome | |
Info: | Partial androgen insensitivity Reifenstein syndrome | |
E34.8 | Other specified endocrine disorders | |
Info: | Pineal gland dysfunction Progeria | |
Excl2.: | pseudohypoparathyroidism (E20.1) | |
E34.9 | Endocrine disorder, unspecified | |
Info: | Endocrine disturbance NOS Hormone disturbance NOS | |
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