OMOP Concept 36714336
Autosomal dominant palmoplantar keratoderma and congenital alopecia
StandardConditionSNOMED719518004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant palmoplantar keratoderma and congenital alopecia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 719518004 | Autosomal dominant palmoplantar keratoderma and congenital alopecia | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant palmoplantar keratoderma and congenital alopecia across source vocabularies.
- Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder)
- Palmoplantar keratoderma and congenital alopecia Stevanovic type
- queratodermia palmoplantar autosómica dominante y alopecia congénita
- queratodermia palmoplantar autosómica dominante y alopecia congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(54)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital alopecia
- 1Congenital ectodermal defect
- 1Developmental hereditary disorder
- 1Hereditary palmoplantar keratoderma
- 2Alopecia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of hair
- 2Congenital malformation
- 2Developmental disorder
- 2Disorder of embryonic structure
- 2Hereditary disease
- 2Hereditary disorder of the integument
- 2Palmoplantar keratoderma
- 3Congenital anomaly of skin
- 3Congenital disease
- 3Disease
- 3Disorder of foot
- 3Disorder of hair
- 3Disorder of hand
- 3Disorder of integument
- 3Disorder of skin of lower limb
- 3Disorder of skin of upper limb
- 3Genetic disease
- 3Hereditary disorder by system
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