OMOP Concept 4077104
Mutilating keratoderma
StandardConditionSNOMED24559001Disorder
Maps from
2
Descendants
1
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Mutilating keratoderma via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133610 | Mutilating keratoderma | Non-standard |
| MeSH | C536457 | Vohwinkel syndrome | Non-standard |
Synonyms
Alternative names recorded for Mutilating keratoderma across source vocabularies.
- Keratoderma hereditarium mutilans
- Mutilating keratoderma (disorder)
- Mutilating keratoderma of Vohwinkel
- queratodermia mutilante
- queratodermia mutilante de Vohwinkel
- queratodermia mutilante (trastorno)
- síndrome de Vohwinkel
- Vohwinkel's mutilating keratoderma
- Vohwinkel syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(58)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital sensorineural hearing loss
- 1Erythrokeratoderma
- 1Hereditary hearing loss
- 1Hereditary palmoplantar keratoderma
- 1Rough skin of hands
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Congenital hearing disorder
- 2Finding of hand region
- 2Hearing loss
- 2Hereditary disorder of the integument
- 2Inherited disorder of keratinization
- 2Palmoplantar keratoderma
- 2Rough skin
- 2Sensorineural hearing loss
- 3Abnormal keratinization
- 3Congenital disease
- 3Disorder of auditory system
- 3Disorder of foot
- 3Disorder of integument
- 3Disorder of keratinization
- 3Disorder of skin of lower limb
- 3Disorder of skin of upper limb
- 3Finding of upper limb
Showing 25 of 58. Retrieve the full set via the API.
Narrower concepts
(1)Included automatically when you query with descendants.
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