Ehlers-Danlos syndrome type 8
Dermatosparaxis EDS (Ehlers-Danlos syndrome)
Ehlers-Danlos syndrome, mental retardation type
Ehlers-Danlos syndrome musculocontractural type
Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness
Defective biosynthesis of proteodermatan sulfate
Familial articular hypermobility syndrome
Ehlers-Danlos syndrome, type 10
Ehlers-Danlos syndrome arthrogryposic type
Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome
Ehlers-Danlos syndrome progeroid type
Arthrochalasia Ehlers-Danlos syndrome
Myopathic EDS (Ehlers-Danlos syndrome)
Congenital humpback
Ehlers-Danlos syndrome Kosho type
Ehlers-Danlos syndrome, familial joint laxity type
B4GALT7-related spondylodysplastic EDS (Ehlers-Danlos syndrome)
Ehlers-Danlos syndrome with platelet dysfunction
Congenital kyphoscoliosis
Familial joint instability syndrome
Human dermatosparaxis EDS VIIC (Ehlers-Danlos syndrome type 7C)
Ehlers-Danlos syndrome spondylocheirodysplastic type
Ehlers-Danlos syndrome, occipital horn type
Defective biosynthesis of proteodermatan sulphate
Ehlers-Danlos syndrome type 6A
Cutis laxa, x-linked
Classical-like Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome, type 5
Familial generalized articular hypermobility
Occipital horn syndrome
Ehlers-Danlos syndrome, type 11
Familial generalised articular hypermobility
Ehlers-Danlos syndrome type 6B
Ehlers-Danlos syndrome type 7
Xylosylprotein 4-beta-galactosyltransferase deficiency
Ehlers-Danlos myopathy overlap syndrome
AEBP1-related Ehlers-Danlos syndrome
Ehlers-Danlos syndrome due to tenascin-X deficiency
Brittle cornea syndrome
Disorder of copper metabolism
Ehlers-Danlos syndrome, type 8
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome
Spondylodysplastic Ehlers-Danlos syndrome
Ehlers-Danlos syndrome type 9 X-linked
Arthrochalasis multiplex congenita
Congenital hunchback
Congenital kyphosis
Periodontal Ehlers-Danlos syndrome
Ehlers-Danlos syndrome type 6
Myopathic Ehlers-Danlos syndrome
Ehlers-Danlos syndrome cardiac valvular type
Galactosyltransferase I deficiency
Periodontitis associated with genetic disorder
Ehlers-Danlos syndrome classic-like type
Ocular scoliotic EDS (Ehlers-Danlos syndrome)
Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type
Ehlers-Danlos syndrome, dysfibronectinaemic
Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency
Familial joint laxity
Arthrochalasia multiplex congenita
Ehlers-Danlos syndrome type V
Spondylocheirodysplastic Ehlers-Danlos syndrome
Ehlers-Danlos syndrome progeroid type 2
Ehlers-Danlos syndrome, periodontitis type
Copper metabolism disorder
Dermatosparaxis Ehlers-Danlos syndrome
Periodontitis co-occurrent with genetic disorder
Ehlers-Danlos syndrome, x-linked skeletal type
Ehlers-Danlos syndrome type 7C
Periodontitis associated with Ehlers-Danlos syndrome type VIII
Ehlers-Danlos syndrome, type 9
X-linked Ehlers-Danlos syndrome
Protocollagen lysyl hydroxylase deficiency
Ehlers-Danlos syndrome type VIII
Ehlers-Danlos syndrome, hydroxylysine-deficient
Hydroxylysine-deficient collagen disease
AEBP1-related EDS (Ehlers-Danlos syndrome)
Ehlers-Danlos syndrome kyphoscoliotic and deafness type
Adducted thumbs, arthrogryposis syndrome, Dundar type
Classical-like Ehlers-Danlos syndrome type 1
Corneal thinning
Ehlers-Danlos syndrome, dysfibronectinemic
Ehlers-Danlos syndrome type XI
Ehlers-Danlos syndrome type VI
SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome
Thin cornea
Ehlers-Danlos syndrome kyphoscoliotic type
Ehlers-Danlos syndrome, lysyl hydroxylase deficient

Frequently Asked Questions

What is the ICD-10 code for other ehlers-danlos syndromes?

The ICD-10-CM code for other ehlers-danlos syndromes is Q79.69. The full clinical description is "Other Ehlers-Danlos syndromes". Q79.69 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q79.69 mean?

ICD-10-CM code Q79.69 represents “Other Ehlers-Danlos syndromes”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q79.69 a billable code?

Yes, Q79.69 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q79.69 in?

Q79.69 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q79.69 map to?

Q79.69 maps to 25 SNOMED CT concepts: 1255121003, 720860004, 55711009, 1251499005, 720861000, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q79.69?

Q79.69 is linked to 1 UMLS Concept Unique Identifier: C5140892. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q79.69 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other ehlers-danlos syndromes 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 Q79.69?

There is no direct ICD-11 mapping available for Q79.69 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.