OMOP Concept 45765483
Congenital cataracts, facial dysmorphism and neuropathy
StandardConditionSNOMED702433001Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital cataracts, facial dysmorphism and neuropathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565822 | Congenital Cataracts, Facial Dysmorphism, And Neuropathy | Non-standard |
Synonyms
Alternative names recorded for Congenital cataracts, facial dysmorphism and neuropathy across source vocabularies.
- cataratas congénitas, dismorfismo facial y neuropatía
- cataratas congénitas, dismorfismo facial y neuropatía (trastorno)
- CCFDN - congenital cataracts, facial dysmorphism and neuropathy
- Congenital cataracts, facial dysmorphism and neuropathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of eye
- 1Congenital anomaly of the peripheral nervous system
- 1Developmental hereditary disorder
- 1Hereditary disorder of nervous system
- 1Hereditary disorder of the visual system
- 2Anomaly of eye
- 2Autosomal hereditary disorder
- 2Congenital anomaly of head
- 2Congenital anomaly of nervous system
- 2Congenital anomaly of visual system
- 2Developmental disorder
- 2Disorder of nervous system
- 2Disorder of the peripheral nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Visual system disorder
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3Disorder of eye
- 3Disorder of head
- 3Eye / vision finding
- 3Genetic disease
- 4Clinical finding
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