ICD-10-CM E34: Other endocrine disorders

pseudohypoparathyroidism (E20.1)

ectopic ACTH syndrome (E24.3)

• 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)

pseudohypoparathyroidism (E20.1)

Carcinoid disease, unspecified

• Carcinoid heart disease
• Hedinger syndrome

• Carcinoid disease NEC
• Carcinoid syndrome NEC
• Other carcinoid disease

Constitutional delay of growth, puberty, or maturation

• 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

• 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

• Short stature due to ACAN gene variant
• Short stature due to aggrecan deficiency
• Short stature due to NPR-2 gene variant

Constitutional gigantism

Androgen insensitivity NOS

• Complete androgen insensitivity
• de Quervain syndrome
• Goldberg-Maxwell syndrome

• Partial androgen insensitivity
• Reifenstein syndrome

• Pineal gland dysfunction
• Progeria

• Endocrine disturbance NOS
• Hormone disturbance NOS

• the underlying disorder, such as:
• primary neuroendocrine tumors (C7A.-)
• secondary neuroendocrine tumors (C7B.-)