OMOP Concept 36716703
PTEN hamartoma tumor syndrome
StandardConditionSNOMED722859001Disorder
Maps from
1
Descendants
4
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to PTEN hamartoma tumor syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | Q85.81 | PTEN hamartoma tumor syndrome | Non-standard |
Synonyms
Alternative names recorded for PTEN hamartoma tumor syndrome across source vocabularies.
- PTEN hamartoma tumor syndrome (disorder)
- PTEN hamartoma tumour syndrome
- síndrome tumoral hamartomatoso asociado a PTEN
- síndrome tumoral hamartomatoso asociado a PTEN (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital hamartoma of skin
- 1Developmental hereditary disorder
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary disorder of the integument
- 1Multiple malformation syndrome with early overgrowth
- 2Autosomal hereditary disorder
- 2Congenital hamartoma
- 2Developmental disorder
- 2Disorder of integument
- 2Fetal and/or neonatal disorder of integument
- 2Hamartoma of skin
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 3Congenital disease
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Fetal and/or neonatal disorder
- 3Genetic disease
- 3Hamartoma
- 3Hamartoma of integument
- 3Integumentary system finding
- 3Mass of skin
Showing 25 of 41. Retrieve the full set via the API.
Narrower concepts
(4)Included automatically when you query with descendants.
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