01
Diseases
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 21
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant
- Standard Disease Name
- rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C563392
- OMIM ID
- 245570
- UMLS ID
- C1832814
- HPO ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
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