E34.328

Billable

Other genetic causes of short stature

Other genetic causes of short stature

Status

Billable / Specific

Block

E20-E35

Parent Code

E34.32

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

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

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Related Codes(3)
E34.321

Primary insulin-like growth factor-1 (IGF-1) deficiency

BillableE34.322

Insulin-like growth factor-1 (IGF-1) resistance

BillableE34.329

Unspecified genetic causes of short stature

Billable
Also Known As / Clinical Terms(215)

SNOMED CT

UMLS

Clinical Terms

  • Congenital anomaly of endocrine ovary
  • DONSON-related microcephaly, short stature, limb abnormalities spectrum
  • MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome
  • Genetic syndromes of diabetes mellitus
  • Hypopituitary dwarfism with failure of development of sexual characteristics
  • Hypoplastic anemia - familial
  • Congenital small adrenal gland
  • Primordial microcephalic dwarfism Crachami type
  • Keratosis follicularis, dwarfism, cerebral atrophy syndrome
  • True dwarfism
  • Hypophyseal infantilism
  • Infantile dwarf
  • Brissaud dwarfism
  • MIRAGE syndrome
  • Ovarian dysgenesis
  • Lorain-Levi dwarfism
  • Microcephalic primordial dwarfism Alazami type
  • Asexual dwarfism
  • Internal carotid artery stenosis
  • Microcephalic primordial dwarfism due to ZNF335 deficiency
  • AMeD (aplastic anaemia, intellectual disability, dwarfism) syndrome
  • Multiple malformation syndrome, moderate short stature, facial with or without genital features
  • Diabetes mellitus associated with genetic syndrome
  • CAH - Congenital adrenal hypoplasia
  • Ghrelin receptor deficiency
  • Aplastic anemia, intellectual disability, dwarfism syndrome
  • Microcephalic osteodysplastic primordial dwarfism Taybi Linder type
  • True dwarf
  • Microcephalic osteodysplastic primordial dwarfism types I and III
  • Dolichocephalic dwarfism
  • Short stature due to NPR-2 gene variant
  • Hereditary acantholytic dermatosis
  • Short stature due to aggrecan deficiency
  • AMeD (aplastic anemia, intellectual disability, dwarfism) syndrome
  • Microcephalic primordial dwarfism, insulin resistance syndrome
  • Brissaud-Meige syndrome
  • Stenosis of intracranial carotid artery
  • Congenital hypoplasia of adrenal gland
  • AMeD syndrome
  • Delayed bone age
  • Short stature with delayed bone age due to thyroid hormone metabolism deficiency
  • Bird-headed dwarfism Montreal type
  • Frohlich dwarfism
  • Nanosomia
  • Autosomal recessive asexual dwarfism
  • Bone age finding
  • Microcephalic primordial dwarfism Toriello type
  • Microcephalic primordial dwarfism of Toriello type
  • Constitutional aplastic anemia
  • Dolichocephalia
  • Dolichocephaly
  • Congenital adrenal hypoplasia
  • Intracranial carotid artery stenosis
  • Short stature due to GHSR deficiency
  • Insulin resistance
  • Microcephalic primordial dwarfism Montreal type
  • Long narrow head
  • Short stature due to growth hormone secretagogue receptor deficiency
  • Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome
  • Body height below reference range
  • Stratton Parker syndrome
  • Primordial dwarfism
  • Taybi Linder syndrome
  • Retarded bone age
  • Normal dwarfism
  • Moyamoya disease
  • Short stature due to GHSR (growth hormone secretagogue receptor) deficiency
  • Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
  • Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency
  • Pfeiffer Palm Teller syndrome
  • Osteodysplastic primordial dwarfism
  • MOPD (microcephalic osteodysplastic primordial dwarfism) type II
  • Burnier syndrome
  • Short stature co-occurrent and due to endocrine disorder
  • Microcephalic primordial dwarfism Dauber type
  • Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome
  • Normal dwarf
  • Dolichocephalism
  • Short stature, wormian bones, dextrocardia syndrome
  • Microcephalic osteodysplastic primordial dwarfism type II
  • Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome
  • Microcephalic primordial dwarfism Walsh type
  • Moyamoya disease, short stature, facial dysmorphism, hypergonadotropic hypogonadism
  • Majewski osteodysplastic primordial dwarfism type II
  • Pure dwarf
  • Pure dwarfism
  • Short stature due to ACAN gene variant
  • Aplastic anaemia, intellectual disability, dwarfism syndrome
  • Alazami syndrome
  • Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
  • Malabsorption of glucose
  • 46,XX ovarian dysgenesis, short stature syndrome
  • Constitutional aplastic anaemia
  • Microcephalic primordial dwarfism due to ZNF335 (zinc finger protein 335) deficiency
  • Congenital aplastic anaemia
  • PPT (Pfeiffer Palm Teller) syndrome
  • DNA replication fork stabilisation factor DONSON-related microcephaly, short stature, limb abnormalities spectrum
  • Mikati Najjar Sahli syndrome
  • Nebecourt syndrome
  • Congenital stenosis of carotid artery
  • ICA - Internal carotid artery stenosis
  • X-linked asexual dwarfism
  • Multiple malformation syndrome, moderate short stature, facial
  • Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome
  • Hypoplastic anaemia - familial
  • Congenital aplastic anemia
  • DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum
Frequently Asked Questions
What is the ICD-10 code for other genetic causes of short stature?

The ICD-10-CM code for other genetic causes of short stature is E34.328. The full clinical description is "Other genetic causes of short stature". E34.328 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E34.328 mean?

ICD-10-CM code E34.328 represents “Other genetic causes of short stature”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E34.328 a billable code?

Yes, E34.328 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E34.328 in?

E34.328 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E34.328?

E34.328 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 12 more.

What SNOMED CT codes does E34.328 map to?

E34.328 maps to 45 SNOMED CT concepts: 1237345002, 1332385000, 770564004, 7530009, 17192009, and 40 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E34.328?

E34.328 is linked to 4 UMLS Concept Unique Identifiers: C5674893, C5676334, C5676336, C5676335. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E34.328 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other genetic causes of short stature affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E34.328?

There is no direct ICD-11 mapping available for E34.328 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.