OMOP Concept 443261
Disorder of keratinization
StandardConditionSNOMED277905003Disorder
Maps from
1
Descendants
170
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Disorder of keratinization via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 277905003 | Disorder of keratinization | Non-standard |
Synonyms
Alternative names recorded for Disorder of keratinization across source vocabularies.
- Disorder of keratinisation
- Disorder of keratinization (disorder)
- trastorno de la queratinización
- trastorno de la queratinización (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(170)Included automatically when you query with descendants.
- 1Acanthosis nigricans
- 1Acquired disorder of keratinization
- 1Drug-induced ichthyosiform reaction
- 1Epidermal dysplasia
- 1Follicular keratosis
- 1Harlequin fetus
- 1Ichthyosis hystrix
- 1Inherited disorder of keratinization
- 1Leukokeratosis
- 1Porokeratosis
- 1Skin peeling disorder
- 1Terra firma-forme dermatosis
- 2Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome
- 2Acanthosis nigricans of oral mucous membranes
- 2Acquired acanthosis nigricans
- 2Acquired ichthyosis
- 2Acquired keratosis follicularis
- 2Acrokeratosis verruciformis of Hopf
- 2Atrophoderma vermiculatum
- 2Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering
- 2Congenital ichthyosis of skin
- 2Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome
- 2Crouzon syndrome with acanthosis nigricans
- 2Cutis gyrata syndrome of Beare and Stevenson
- 2Desquamation of skin following febrile illness
- 2Desquamation secondary to acute systemic illness
- 2Diffuse palmoplantar keratoderma with painful fissures
- 2Disseminated superficial actinic porokeratosis
- 2Disseminated superficial porokeratosis
- 2Drug-induced desquamation of skin
- 2Erythrokeratoderma
- 2Familial benign pemphigus
- 2Focal palmoplantar keratoderma with joint keratoses
- 2Follicular ichthyosis
- 2Hereditary acantholytic dermatosis
- 2Hereditary erythrokeratolysis
- 2Hereditary follicular keratoses
- 2Hereditary skin peeling syndrome
- 2Hyperkeratosis follicularis in cutem penetrans
- 2Hyperkeratosis lenticularis perstans
- 2Ichthyosis hystrix Bäfverstedt type
- 2Ichthyosis hystrix gravior
- 2Ichthyosis hystrix of Curth-Macklin
- 2Keratosis circumscripta
- 2Keratosis follicularis, dwarfism, cerebral atrophy syndrome
- 2Keratosis pilaris
- 2Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome
- 2Lelis syndrome
- 2Leukoencephalopathy, palmoplantar keratoderma syndrome
- 2Leukokeratosis of skin
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