01
Diseases
20p12.3 microdeletion syndrome
20p12.3 microdeletion syndrome
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
Basic Information
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Core Information
- Disease Name
- 20p12.3 microdeletion syndrome
- Standard Disease Name
- 20p12.3 microdeletion syndrome
- MeSH Tree
- No data
- ICD-10
- Q93.5
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- No data
- UMLS ID
- No data
- HPO ID
- No data
Description and Extensions
- Description
- 20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome (see this term), variable developmental delay and facial dysmorphism.
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