OMOP Concept 4220949
Papillon-Lefèvre syndrome
StandardConditionSNOMED40158001Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Papillon-Lefèvre syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 130911 | Papillon-Lefèvre syndrome | Non-standard |
| MeSH | D010214 | Papillon-Lefevre Disease | Non-standard |
Synonyms
Alternative names recorded for Papillon-Lefèvre syndrome across source vocabularies.
- Juvenile periodontosis with hyperkeratosis
- Papillon-Lefevre syndrome
- Papillon-Lefèvre syndrome (disorder)
- periodontosis juvenil con hiperqueratosis
- síndrome de Papillon - Lefèvre
- síndrome de Papillon - Lefèvre (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(100)Roll up to these when you need a wider cohort.
- 1Alveolar bone loss
- 1Autosomal recessive hereditary disorder
- 1Congenital abnormality of oral cavity
- 1Congenital anomaly of face bones
- 1Congenital anomaly of foot
- 1Congenital anomaly of hand
- 1Congenital anomaly of jaw
- 1Developmental hereditary disorder
- 1Digestive system hereditary disorder
- 1Ectodermal dysplasia
- 1Hereditary diffuse palmoplantar keratoderma
- 1Hereditary disorder of musculoskeletal system
- 1Structural abnormality of bone structure of jaw
- 2Autosomal hereditary disorder
- 2Congenital anomaly of bone of head
- 2Congenital anomaly of face
- 2Congenital anomaly of head
- 2Congenital anomaly of lower limb
- 2Congenital anomaly of mouth
- 2Congenital anomaly of upper limb
- 2Congenital ectodermal defect
- 2Congenital malformation of upper alimentary tract
- 2Developmental disorder
- 2Disorder of digestive system
- 2Disorder of facial bone
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