OMOP Concept 36714656
Haim Munk syndrome
StandardConditionSNOMED719973009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Haim Munk syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537627 | Keratosis palmoplantaris with periodontopathia and onychogryposis | Non-standard |
| Nebraska Lexicon | 719973009 | Keratosis palmoplantaris with periodontopathia and onychogryposis syndrome | Non-standard |
Synonyms
Alternative names recorded for Haim Munk syndrome across source vocabularies.
- Haim Munk syndrome (disorder)
- Keratosis palmoplantaris with periodontopathia and onychogryposis syndrome
- síndrome de Haim Munk
- síndrome de Haim Munk (trastorno)
- síndrome de queratosis palmoplantar con periodontopatía y onicogriposis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(78)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of skin
- 1Congenital anomaly of tooth
- 1Developmental hereditary disorder
- 1Hereditary diffuse palmoplantar keratoderma
- 1Hereditary disorder of tooth
- 1Multiple system malformation syndrome
- 2Autosomal hereditary disorder
- 2Congenital abnormality of oral cavity
- 2Congenital anomaly of digestive organ
- 2Congenital anomaly of integument
- 2Congenital anomaly of jaw
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Disorder of skin
- 2Hereditary disease
- 2Hereditary palmoplantar keratoderma
- 2Malformation of tooth
- 2Tooth disorder
- 3Congenital anomaly of digestive system
- 3Congenital anomaly of head
- 3Congenital anomaly of mouth
- 3Congenital malformation
- 3Disease
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