OMOP Concept 4301300
Ichthyosis, cerebellar degeneration and hepatosplenomegaly
StandardConditionSNOMED403779009Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Ichthyosis, cerebellar degeneration and hepatosplenomegaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535727 | Dykes Markes Harper syndrome | Non-standard |
| Nebraska Lexicon | 403779009 | Ichthyosis, cerebellar degeneration and hepatosplenomegaly | Non-standard |
Synonyms
Alternative names recorded for Ichthyosis, cerebellar degeneration and hepatosplenomegaly across source vocabularies.
- Ichthyosis, cerebellar degeneration and hepatosplenomegaly (disorder)
- ictiosis, degeneración cerebelosa y hepatoesplenomegalia
- ictiosis, degeneración cerebelosa y hepatoesplenomegalia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Cutaneous syndrome with ichthyosis
- 2Congenital ichthyosis of skin
- 3Developmental hereditary disorder
- 3Genodermatosis
- 3Ichthyosis
- 3Inherited disorder of keratinization
- 3Rough skin
- 4Abnormal keratinization
- 4Congenital anomaly of skin
- 4Developmental disorder
- 4Disorder of keratinization
- 4Hereditary disease
- 4Hereditary disorder of the integument
- 4Keratoderma
- 4Skin finding
- 5Congenital anomaly of integument
- 5Disease
- 5Disorder of integument
- 5Disorder of skin
- 5Functional finding
- 5General finding of soft tissue
- 5Genetic disease
- 5Hereditary disorder by system
- 5Integumentary system finding
- 5Keratosis
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