Category · FY2027
E34 Other endocrine disorders
- Header · not billable
E34 is not billable. The category heads 18 billable codes in FY2027, grouped under 8 subdivisions.
Index → code
Where it sits
- Billable codes
- 18
- Subdivisions
- 8
- CC / MCC codes
- 3 / 0
- HCC V28 codes
- 3
- New FY2027
- 0
- Index entries
- 119
Codes in E34
- E34.0
- E34.00Carcinoid syndrome, unspecifiedBillableCC17
Inclusion terms 1
Inclusion terms
- Carcinoid disease, unspecified
- E34.01Carcinoid heart syndromeBillableCC17
Inclusion terms 2
Inclusion terms
- Carcinoid heart disease
- Hedinger syndrome
- E34.09Other carcinoid syndromeBillableCC17
Inclusion terms 3
Inclusion terms
- Carcinoid disease NEC
- Carcinoid syndrome NEC
- Other carcinoid disease
- E34.1Other hypersecretion of intestinal hormonesBillable
- E34.2Ectopic hormone secretion, not elsewhere classifiedBillable
Excludes1 1
Excludes1
- ectopic ACTH syndrome (E24.3) E24.3
- E34.3Short stature due to endocrine disorderHeader
Excludes1 11
Excludes1
- achondroplastic short stature (Q77.4) Q77.4
- hypochondroplastic short stature (Q77.4) Q77.4
- nutritional short stature (E45) E45
- pituitary short stature (E23.0) E23.0
- progeria (E34.8) E34.8
- renal short stature (N25.0) N25.0
- Russell-Silver syndrome (Q87.19) Q87.19
- short-limbed stature with immunodeficiency (D82.2) D82.2
- short stature (child) (R62.52) R62.52
- short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
- short stature NOS (R62.52) R62.52
- E34.30Short stature due to endocrine disorder, unspecifiedBillable
- E34.31Constitutional short statureBillable
Inclusion terms 1
Inclusion terms
- Constitutional delay of growth, puberty, or maturation
- E34.32Genetic causes of short statureHeader
- E34.321Primary insulin-like growth factor-1 (IGF-1) deficiencyBillable
Inclusion terms 7
Inclusion terms
- 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
- E34.322Insulin-like growth factor-1 (IGF-1) resistanceBillable
Inclusion terms 3
Inclusion terms
- 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
- E34.328Other genetic causes of short statureBillable
Inclusion terms 3
Inclusion terms
- Short stature due to ACAN gene variant
- Short stature due to aggrecan deficiency
- Short stature due to NPR-2 gene variant
- E34.329Unspecified genetic causes of short statureBillable
- E34.39Other short stature due to endocrine disorderBillable
- E34.4Constitutional tall statureBillable
Inclusion terms 1
Inclusion terms
- Constitutional gigantism
- E34.5Androgen insensitivity syndromeHeader
- E34.50Androgen insensitivity syndrome, unspecifiedBillable
Inclusion terms 1
Inclusion terms
- Androgen insensitivity NOS
- E34.51Complete androgen insensitivity syndromeBillable
Inclusion terms 3
Inclusion terms
- Complete androgen insensitivity
- de Quervain syndrome
- Goldberg-Maxwell syndrome
- E34.52Partial androgen insensitivity syndromeBillable
Inclusion terms 2
Inclusion terms
- Partial androgen insensitivity
- Reifenstein syndrome
- E34.8Other specified endocrine disordersBillable
Inclusion terms 2, Excludes2 1
Inclusion terms
- Pineal gland dysfunction
- Progeria
Excludes2
- pseudohypoparathyroidism (E20.1) E20.1
- E34.9Endocrine disorder, unspecifiedBillable
Inclusion terms 2
Inclusion terms
- Endocrine disturbance NOS
- Hormone disturbance NOS
CC/MCC: as a secondary diagnosis, unless the principal diagnosis is on the code’s PDX exclusion list (MS-DRG v44 Appendix C; list on the code card).
Instructions
At E34
Excludes1
- pseudohypoparathyroidism (E20.1) E20.1
Notes that also apply
Block E20-E35 instructions (Excludes1 2): printed on the block page.
Chapter 4 instructions (Notes 1, Excludes1 1): printed on the chapter 4 page.
Index entries
- Carcinoidosis → E34.00
- Björck (-Thorson) syndrome (malignant carcinoid) → E34.09
- Cassidy (-Scholte) syndrome (malignant carcinoid) → E34.09
- Flush syndrome → E34.09
- Scholte's syndrome (malignant carcinoid) → E34.09
- Thorson-Björck syndrome → E34.09
- Dwarfism → E34.328
- Tall stature, constitutional → E34.4
- Androgen insensitivity syndrome → E34.50
- Androgen resistance syndrome → E34.50
- Goldberg-Maxwell syndrome → E34.51
- Reifenstein syndrome → E34.52
- Donohue's syndrome → E34.8
- Gilford-Hutchinson disease → E34.8
- Hutchinson-Gilford disease or syndrome → E34.8
- Hyperpinealism → E34.8
- Hypopinealism → E34.8
- Leprechaunism → E34.8
- Pellizzi's syndrome → E34.8
- Progeria → E34.8
- Werner's disease or syndrome → E34.8
- Dysendocrinism → E34.9
- Disease, diseased›carcinoid → E34.00
- Syndrome›carcinoid → E34.00
- Syndrome›metastatic carcinoid → E34.00
- Carcinoidosis›heart → E34.01
- Syndrome›Hedinger's → E34.01
- Argentaffinoma›syndrome → E34.09
- Syndrome›argentaffin, argintaffinoma → E34.09
- Syndrome›Björck (-Thorsen) → E34.09
- Syndrome›Cassidy (-Scholte) → E34.09
- Syndrome›flush → E34.09
- Syndrome›Scholte's → E34.09
- Syndrome›Thorson-Björck → E34.09
- Ectopic, ectopia (congenital)›hormone secretion NEC → E34.2
- Dwarfism›constitutional → E34.31
- Dwarfism›Laron-type → E34.321
- Dwarfism›congenital → E34.328
- Dwarfism›infantile → E34.328
- Gigantism (cerebral) (hypophyseal) (pituitary)›constitutional → E34.4
79 more, longer entries are not listed; the search box finds them by word.
NCHS Alphabetic Index. Index first, then the Tabular List.