OMOP Concept 4271018
Hereditary diffuse palmoplantar keratoderma
StandardConditionSNOMED400123002Disorder
Maps from
4
Descendants
24
Valid from
31 Jul 2003
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Hereditary diffuse palmoplantar keratoderma via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138791 | Diffuse palmoplantar keratoderma | Non-standard |
| HPO | HP_0007447 | Diffuse palmoplantar hyperkeratosis | Non-standard |
| MeSH | D015776 | Keratoderma, Palmoplantar, Diffuse | Non-standard |
| Read | PH3y600 | Keratosis palmaris et plantaris | Non-standard |
Synonyms
Alternative names recorded for Hereditary diffuse palmoplantar keratoderma across source vocabularies.
- Diffuse palmoplantar keratoderma
- Hereditary diffuse palmoplantar keratoderma (disorder)
- queratodermia palmoplantar difusa hereditaria
- queratodermia palmoplantar difusa hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(37)Roll up to these when you need a wider cohort.
- 1Hereditary palmoplantar keratoderma
- 2Hereditary disorder of the integument
- 2Palmoplantar keratoderma
- 3Disorder of foot
- 3Disorder of integument
- 3Disorder of skin of lower limb
- 3Disorder of skin of upper limb
- 3Hereditary disorder by system
- 3Keratoderma
- 3Structural abnormality of hand
- 4Disorder of body system
- 4Disorder of free lower limb
- 4Disorder of hand
- 4Disorder of skin
- 4Disorder of soft tissue of lower limb
- 4Disorder of soft tissue of upper limb
- 4Finding of foot region
- 4Hereditary disease
- 4Integumentary system finding
- 4Keratosis
- 5Clinical finding
- 5Disease
- 5Disorder of lower limb
- 5Disorder of skin and/or subcutaneous tissue
- 5Disorder of soft tissue of limb
Showing 25 of 37. Retrieve the full set via the API.
Narrower concepts
(24)Included automatically when you query with descendants.
- 1Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type
- 1CEDNIK syndrome
- 1Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome
- 1Curly hair, acral keratoderma, caries syndrome
- 1Diffuse palmoplantar keratoderma and acrocyanosis syndrome
- 1Diffuse palmoplantar keratoderma of Thost-Unna
- 1Diffuse palmoplantar keratoderma with painful fissures
- 1Epidermolytic palmoplantar keratoderma of Vorner
- 1Haim Munk syndrome
- 1Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome
- 1Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome
- 1Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome
- 1KRT1-related diffuse nonepidermolytic keratoderma
- 1Mal de Meleda
- 1Palmoplantar hyperkeratosis sclerodactyly syndrome
- 1Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome
- 1Palmoplantar keratoderma Nagashima type
- 1Palmoplantar keratoderma transgrediens
- 1Palmoplantar keratoderma with clinodactyly syndrome
- 1Papillon-Lefèvre syndrome
- 1Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome
- 1Progressive palmoplantar keratoderma of Greither
- 1Schöpf-Schulz-Passarge syndrome
- 1Skin fragility, wooly hair, palmoplantar keratoderma syndrome
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