Diagnosis Code: E34.328

Short Description: Other genetic causes of short stature

Long Description: Other genetic causes of short stature

The code E34.328 is VALID for claim submission

Code Classification:

• Endocrine, nutritional and metabolic diseases (E00–E89)
  • Disorders of other endocrine glands (E20-E35)
    • Other endocrine disorders (E34)
      • E34.328 Other genetic causes of short stature

Code Version: 2022 ICD-10-CM

Synonyms

• 46,XX ovarian dysgenesis, short stature syndrome
• 46,XY disorder of sex development
• Asexual dwarfism
• Asexual dwarfism
• Autosomal recessive asexual dwarfism
• Bone age finding
• Congenital anomaly of endocrine ovary
• Congenital hypoplasia of adrenal gland
• Congenital stenosis of carotid artery
• Delayed bone age
• Dolichocephalic dwarfism
• DONSON-related microcephaly, short stature, limb abnormalities spectrum
• Glucose-galactose malabsorption
• Glucose-galactose malabsorption
• Hereditary acantholytic dermatosis
• Infantile dwarf
• Insulin resistance
• Insulin resistance
• Internal carotid artery stenosis
• Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome
• Keratosis follicularis, dwarfism, cerebral atrophy syndrome
• Long narrow head
• Malabsorption of glucose
• Malabsorption of glucose
• Microcephalic osteodysplastic primordial dwarfism type II
• Microcephalic osteodysplastic primordial dwarfism types I and III
• Microcephalic primordial dwarfism Alazami type
• Microcephalic primordial dwarfism Dauber type
• Microcephalic primordial dwarfism due to ZNF335 deficiency
• Microcephalic primordial dwarfism Montreal type
• Microcephalic primordial dwarfism Toriello type
• Microcephalic primordial dwarfism, insulin resistance syndrome
• Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
• MIRAGE syndrome
• Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
• Moyamoya disease
• Multiple malformation syndrome, moderate short stature, facial
• Osteodysplastic primordial dwarfism
• Osteodysplastic primordial dwarfism
• Ovarian dysgenesis
• Primordial dwarfism
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Short stature co-occurrent and due to endocrine disorder
• Short stature due to growth hormone secretagogue receptor deficiency
• Short stature with delayed bone age due to thyroid hormone metabolism deficiency
• Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome
• Short stature, wormian bones, dextrocardia syndrome
• X-linked asexual dwarfism

Diagnostic Related Group(s)

The code E34.328 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Endocrine Disorders With Mcc (643)
• Endocrine Disorders With Cc (644)
• Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code E34.328 has the following ICD-10-CM references to the Index of Diseases and Injuries

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

Similar Codes

This page was last updated on: 10/1/2023

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