Q80.8
BillableOther congenital ichthyosis
Other congenital ichthyosis
Status
Billable / Specific
Parent Code
Q80Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Chanarin-Dorfman disease19604005
- Chanarin-Miranda syndrome19604005
- Ichthyosiform erythroderma with leucocyte vacuolation19604005
- Ichthyosiform erythroderma with leukocyte vacuolation19604005
- Ichthyotic neutral lipid storage disease19604005
- Lipid storage myopathy AND congenital ichthyosis19604005
- Neutral lipid storage disease19604005
- Triglyceride storage disease with ichthyosis19604005
- Bamboo hair22486004
- Trichoclasis22486004
- Trichorrhexis invaginata22486004
- Ichthyosis linearis circumflexa54336006
- Ichthyosis hystrix67510007
- Trichorrhexis68609006
- HIES - hyperimmunoglobulin E syndrome191009009
- Hyper-IgE syndrome191009009
- Hyperimmunoglobulin E syndrome191009009
- Follicular ichthyosis238627002
- Cutaneous syndrome with ichthyosis239057002
- Ichthyosis hystrix Rheydt type239059004
- KID syndrome239059004
- KID/HID syndrome239059004
- KIDS - Keratitis ichthyosis and deafness syndrome239059004
- Keratitis ichthyosis and deafness syndrome239059004
- Keratitis ichthyosis deafness syndrome239059004
- Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome239059004
- Atypical ichthyosis vulgaris with hypogonadism239060009
- Ichthyosis vulgaris254157005
- BIE - Bullous ichthyosiform erythroderma254167000
- Bullous ichthyosiform erythroderma254167000
- Bullous ichthyosis254167000
- Congenital bullous ichthyosiform erythroderma254167000
- Dominant ichthyosis vulgaris254167000
- Epidermolytic hyperkeratosis254167000
- Ichthyosis hystrix of Curth-Macklin254170001
- Ichthyosis hystrix Bäfverstedt type254171002
- Maleformatio ectodermalis generalisata of Bafverstedt254171002
- Axial osteosclerosis with bamboo hair312514006
- Comel-Netherton syndrome312514006
- Netherton syndrome312514006
- Netherton's syndrome312514006
- Xeroderma in genetic syndrome402600008
- Autosomal dominant ichthyosis402770002
- Autosomal recessive ichthyosis402772005
- Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome403780007
- Autosomal recessive keratitis-ichthyosis-deafness syndrome403780007
- IFAP - ichthyosis follicularis with alopecia and photophobia403782004
- Ichthyosis follicularis with alopecia and photophobia403782004
- Ichthyosis follicularis with alopecia and photophobia (IFAP)403782004
- ICE (ichthyosis cheek eyebrow) syndrome716097001
- Ichthyosis cheek eyebrow syndrome716097001
- Sidransky Feinstein Goodman syndrome716097001
- Annular epidermolytic ichthyosis718631006
- CHIME (coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, ear anomaly) syndrome720639008
- CHIME syndrome720639008
- Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome720639008
- Neuroectodermal dysplasia CHIME type720639008
- Zunich Kaye syndrome720639008
- Keratinopathic ichthyosis724837004
- Genetically determined skin fragility724851004
- Hereditary skin fragility724851004
- Congenital ichthyosis type 4763401009
- Ichthyosis prematurity syndrome763401009
- Autosomal recessive exfoliative ichthyosis763768001
- Exfoliative ichthyosis763768001
- Ichthyosis exfoliativa763768001
- KLICK syndrome763775000
- Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome763775000
- Trichodysplasia xeroderma syndrome766812005
- Autosomal recessive epidermolytic ichthyosis890235002
- Ichthyosis Lambert type1255143006
- Ichthyosis hystrix gravior1255143006
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.