Excludes1

  1. E34 Other endocrine disorders

    Excludes1

    • pseudohypoparathyroidism (E20.1)
    1. E34.0 Carcinoid syndrome

      Note: May be used as an additional code to identify functional activity associated with a carcinoid tumor.

    2. E34.1 Other hypersecretion of intestinal hormones

    3. E34.2 Ectopic hormone secretion, not elsewhere classified

    4. E34.3 Short stature due to endocrine disorder

      1. E34.30 Short stature due to endocrine disorder, unspecified

      2. E34.31 Constitutional short stature

        Inclusion term(s):

        • Constitutional delay of growth, puberty, or maturation
      3. E34.32 Genetic causes of short stature

        • E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency

          Inclusion term(s):

          • 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

          Inclusion term(s):

          • 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

          Inclusion term(s):

          • 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
      4. E34.39 Other short stature due to endocrine disorder

    5. E34.4 Constitutional tall stature

      Inclusion term(s):

      • Constitutional gigantism
    6. E34.5 Androgen insensitivity syndrome

      1. E34.50 Androgen insensitivity syndrome, unspecified

        Inclusion term(s):

        • Androgen insensitivity NOS
      2. E34.51 Complete androgen insensitivity syndrome

        Inclusion term(s):

        • Complete androgen insensitivity
        • de Quervain syndrome
        • Goldberg-Maxwell syndrome
      3. E34.52 Partial androgen insensitivity syndrome

        Inclusion term(s):

        • Partial androgen insensitivity
        • Reifenstein syndrome
    7. E34.8 Other specified endocrine disorders

      Inclusion term(s):

      • Pineal gland dysfunction
      • Progeria
    8. E34.9 Endocrine disorder, unspecified

      Inclusion term(s):

      • Endocrine disturbance NOS
      • Hormone disturbance NOS
Abbreviations used here:

NEC Not elsewhere classifiable
This abbreviation in the Tabular List represents “other specified”. When a specific code is not available for a condition, the Tabular List includes an NEC entry under a code to identify the code as the “other specified” code.

NOS Not otherwise specified
This abbreviation is the equivalent of unspecified.