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- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 5
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
- Bardet-Biedl Syndrome 10
- Standard Disease Name
- bardet-biedl syndrome 10
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D037081
- OMIM ID
- No data
- UMLS ID
- C1136154
- HPO ID
- No data
Description and Extensions
- Description
- MSH2017_2016_08_12:A condition characterized by a broad range of progressive disorders ranging from TENOSYNOVITIS to tendon rupture with or without hindfoot collapse to a fixed, rigid, FLATFOOT deformity. Pathologic changes can involve associated tendons, ligaments, joint structures of the ANKLE, hindfoot, and midfoot. Posterior tibial tendon dysfunction is the most common cause of acquired flatfoot deformity in adults.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target2 Ingredients
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