ICE (ichthyosis cheek eyebrow) syndrome
Autosomal recessive exfoliative ichthyosis
Ichthyosiform erythroderma with leukocyte vacuolation
Cutaneous syndrome with ichthyosis
Ichthyotic neutral lipid storage disease
KLICK syndrome
Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome
IFAP - ichthyosis follicularis with alopecia and photophobia
Xeroderma in genetic syndrome
Ichthyosis hystrix
CHIME syndrome
Follicular ichthyosis
Exfoliative ichthyosis
Ichthyosis exfoliativa
Congenital bullous ichthyosiform erythroderma
Keratitis ichthyosis and deafness syndrome
Lipid storage myopathy AND congenital ichthyosis
Hyper-IgE syndrome
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome
Sidransky Feinstein Goodman syndrome
BIE - Bullous ichthyosiform erythroderma
Trichorrhexis invaginata
Autosomal recessive keratitis-ichthyosis-deafness syndrome
Neuroectodermal dysplasia CHIME type
Hereditary skin fragility
Ichthyosis follicularis with alopecia and photophobia (IFAP)
Ichthyosis hystrix gravior
Trichodysplasia xeroderma syndrome
Triglyceride storage disease with ichthyosis
Zunich Kaye syndrome
Bullous ichthyosis
Autosomal recessive epidermolytic ichthyosis
KID/HID syndrome
Atypical ichthyosis vulgaris with hypogonadism
Dominant ichthyosis vulgaris
Ichthyosis hystrix Bäfverstedt type
KIDS - Keratitis ichthyosis and deafness syndrome
Netherton's syndrome
Trichorrhexis
Genetically determined skin fragility
Chanarin-Miranda syndrome
Congenital ichthyosis type 4
Ichthyosiform erythroderma with leucocyte vacuolation
Ichthyosis hystrix Rheydt type
CHIME (coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, ear anomaly) syndrome
Ichthyosis linearis circumflexa
Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome
Ichthyosis vulgaris
KID syndrome
Keratinopathic ichthyosis
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome
Neutral lipid storage disease
Ichthyosis hystrix of Curth-Macklin
Chanarin-Dorfman disease
Autosomal dominant ichthyosis
Bamboo hair
Trichoclasis
Annular epidermolytic ichthyosis
HIES - hyperimmunoglobulin E syndrome
Ichthyosis Lambert type
Hyperimmunoglobulin E syndrome
Autosomal recessive ichthyosis
Epidermolytic hyperkeratosis
Bullous ichthyosiform erythroderma
Netherton syndrome
Ichthyosis follicularis with alopecia and photophobia
Axial osteosclerosis with bamboo hair
Keratitis ichthyosis deafness syndrome
Maleformatio ectodermalis generalisata of Bafverstedt
Ichthyosis prematurity syndrome
Comel-Netherton syndrome
Ichthyosis cheek eyebrow syndrome

Frequently Asked Questions

What is the ICD-10 code for other congenital ichthyosis?

The ICD-10-CM code for other congenital ichthyosis is Q80.8. The full clinical description is "Other congenital ichthyosis". Q80.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q80.8 mean?

ICD-10-CM code Q80.8 represents “Other congenital ichthyosis”. 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 Q80.8 a billable code?

Yes, Q80.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q80.8 in?

Q80.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q80.8?

Q80.8 has Excludes1 notes indicating codes that cannot be used together with it, including: Refsum's disease (G60.1).

What SNOMED CT codes does Q80.8 map to?

Q80.8 maps to 31 SNOMED CT concepts: 718631006, 239060009, 402770002, 403780007, 890235002, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q80.8?

Q80.8 is linked to 1 UMLS Concept Unique Identifier: C0478084. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q80.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital ichthyosis 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 Q80.8?

Q80.8 maps to the ICD-11 code: EC20.Y (Other specified genetic disorders of keratinisation).

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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.