E34.328
BillableOther genetic causes of short stature
Other genetic causes of short stature
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)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- galactorrhea (N64.3)
- gynecomastia (N62)
- pseudohypoparathyroidism (E20.1)
- 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)
Also Known As / Clinical Terms
SNOMED CT
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Asexual dwarfism7530009
- Brissaud dwarfism7530009
- Brissaud-Meige syndrome7530009
- Burnier syndrome7530009
- Frohlich dwarfism7530009
- Hypophyseal infantilism7530009
- Hypopituitary dwarfism with failure of development of sexual characteristics7530009
- Lorain-Levi dwarfism7530009
- Nebecourt syndrome7530009
- Autosomal recessive asexual dwarfism17192009
- Infantile dwarf21265004
- Congenital aplastic anaemia28975000
- Congenital aplastic anemia28975000
- Constitutional aplastic anaemia28975000
- Constitutional aplastic anemia28975000
- Hypoplastic anaemia - familial28975000
- Hypoplastic anemia - familial28975000
- Dolichocephalic dwarfism39401000
- X-linked asexual dwarfism57536002
- Moyamoya disease69116000
- Dolichocephalia72239002
- Dolichocephalism72239002
- Dolichocephaly72239002
- Long narrow head72239002
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- CAH - Congenital adrenal hypoplasia93235007
- Congenital adrenal hypoplasia93235007
- Congenital hypoplasia of adrenal gland93235007
- Congenital small adrenal gland93235007
- Congenital stenosis of carotid artery93396008
- Delayed bone age123983008
- Retarded bone age123983008
- Ovarian dysgenesis205683001
- ICA - Internal carotid artery stenosis233964008
- Internal carotid artery stenosis233964008
- Nanosomia237837007
- Normal dwarf237837007
- Normal dwarfism237837007
- Primordial dwarfism237837007
- Pure dwarf237837007
- Pure dwarfism237837007
- True dwarf237837007
- True dwarfism237837007
- Osteodysplastic primordial dwarfism254101001
- Hereditary acantholytic dermatosis254217002
- Malabsorption of glucose267426009
- Congenital anomaly of endocrine ovary370966000
- Bone age finding397651006
- Microcephalic primordial dwarfism Toriello type715482004
- Microcephalic primordial dwarfism of Toriello type715482004
- Keratosis follicularis, dwarfism, cerebral atrophy syndrome723830005
- Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome724097003
- Moyamoya disease, short stature, facial dysmorphism, hypergonadotropic hypogonadism724097003
- Microcephalic primordial dwarfism Walsh type724141003
- Microcephalic primordial dwarfism due to ZNF335 (zinc finger protein 335) deficiency724141003
- Microcephalic primordial dwarfism due to ZNF335 deficiency724141003
- Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency724141003
- Microcephalic osteodysplastic primordial dwarfism Taybi Linder type725461009
- Microcephalic osteodysplastic primordial dwarfism types I and III725461009
- Primordial microcephalic dwarfism Crachami type725461009
- Taybi Linder syndrome725461009
- PPT (Pfeiffer Palm Teller) syndrome726672000
- Pfeiffer Palm Teller syndrome726672000
- Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome726672000
- Microcephalus, hypergonadotropic hypogonadism, short stature syndrome733092009
- Mikati Najjar Sahli syndrome733092009
- Insulin resistance763325000
- Short stature, wormian bones, dextrocardia syndrome763631006
- Stratton Parker syndrome763631006
- Short stature with delayed bone age due to thyroid hormone metabolism deficiency763890006
- Bird-headed dwarfism Montreal type765758008
- Microcephalic primordial dwarfism Montreal type765758008
- Ghrelin receptor deficiency766817004
- Short stature due to GHSR (growth hormone secretagogue receptor) deficiency766817004
- Short stature due to GHSR deficiency766817004
- Short stature due to growth hormone secretagogue receptor deficiency766817004
- Alazami syndrome770564004
- Microcephalic primordial dwarfism Alazami type770564004
- Microcephalic primordial dwarfism Dauber type770565003
- Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome1197592001
- MOPD (microcephalic osteodysplastic primordial dwarfism) type II1208348002
- Majewski osteodysplastic primordial dwarfism type II1208348002
- Microcephalic osteodysplastic primordial dwarfism type II1208348002
- Microcephalic primordial dwarfism, insulin resistance syndrome1220596009
- MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome1234831009
- MIRAGE syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome1234831009
- DNA replication fork stabilisation factor DONSON-related microcephaly, short stature, limb abnormalities spectrum1236845001
- DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum1236845001
- DONSON-related microcephaly, short stature, limb abnormalities spectrum1236845001
- 46,XX ovarian dysgenesis, short stature syndrome1237345002
- AMeD (aplastic anaemia, intellectual disability, dwarfism) syndrome1332385000
- AMeD (aplastic anemia, intellectual disability, dwarfism) syndrome1332385000
- AMeD syndrome1332385000
- Aplastic anaemia, intellectual disability, dwarfism syndrome1332385000
- Aplastic anemia, intellectual disability, dwarfism syndrome1332385000
- Body height below reference range1363478003
- Intracranial carotid artery stenosis450440061000119108
- Stenosis of intracranial carotid artery450440061000119108
- Short stature co-occurrent and due to endocrine disorder368331000119100
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.
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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.