01
HDAC6
No data
Diseases
X-Linked Dominant Chondrodysplasia, Chassaing-Lacombe Type
x-linked dominant chondrodysplasia, chassaing-lacombe type
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
Basic Information
Grouped by core information, identifiers, and descriptions.
Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.
Core Information
- Disease Name
- X-Linked Dominant Chondrodysplasia, Chassaing-Lacombe Type
- Standard Disease Name
- x-linked dominant chondrodysplasia, chassaing-lacombe type
- MeSH Tree
- No data
- ICD-10
- Q87.8
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 300863
- UMLS ID
- No data
- HPO ID
- No data
Description and Extensions
- Description
- X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease1 Targets