OMOP Concept 36717541
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome
StandardConditionSNOMED722202006Disorder
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 Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 722202006 | Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome | Non-standard |
Synonyms
Alternative names recorded for Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome across source vocabularies.
- Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder)
- síndrome de queratodermia palmoplantar, inversión sexual 46,XX y predisposición al carcinoma escamocelular
- síndrome de queratodermia palmoplantar, inversión sexual 46,XX y predisposición al carcinoma escamocelular (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(63)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of skin
- 1Developmental hereditary disorder
- 1Gonadal dysgenesis
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary diffuse palmoplantar keratoderma
- 1Reproductive system hereditary disorder
- 2Autosomal hereditary disorder
- 2Congenital anomaly of integument
- 2Congenital malformation of genital organs
- 2Developmental disorder
- 2Disorder of reproductive system
- 2Disorder of skin
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary palmoplantar keratoderma
- 3Congenital malformation
- 3Disease
- 3Disorder involving the integument of fetus OR newborn
- 3Disorder of body system
- 3Disorder of skin and/or subcutaneous tissue
- 3Disorder of the genitourinary system
- 3Genetic disease
- 3Genital finding
- 3Genitourinary congenital anomalies
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