OMOP Concept 37397176
Hereditary palmoplantar keratoderma Gamborg Nielsen type
StandardConditionSNOMED717228004Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary palmoplantar keratoderma Gamborg Nielsen type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 717228004 | Hereditary palmoplantar keratoderma Gamborg Nielsen type | Non-standard |
Synonyms
Alternative names recorded for Hereditary palmoplantar keratoderma Gamborg Nielsen type across source vocabularies.
- Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder)
- queratodermia palmoplantar hereditaria, tipo Gamborg Nielsen
- queratodermia palmoplantar hereditaria, tipo Gamborg Nielsen (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Hereditary diffuse palmoplantar keratoderma
- 2Autosomal hereditary disorder
- 2Hereditary palmoplantar keratoderma
- 3Hereditary disease
- 3Hereditary disorder of the integument
- 3Palmoplantar keratoderma
- 4Disorder of foot
- 4Disorder of hand
- 4Disorder of integument
- 4Disorder of skin of lower limb
- 4Disorder of skin of upper limb
- 4Genetic disease
- 4Hereditary disorder by system
- 4Keratoderma
- 5Disease
- 5Disorder of body system
- 5Disorder of free lower limb
- 5Disorder of skin
- 5Disorder of soft tissue of lower limb
- 5Disorder of soft tissue of upper limb
- 5Disorder of upper limb
- 5Finding of foot region
- 5Finding of hand region
- 5Integumentary system finding
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