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Diseases
Craniometaphyseal Dysplasia, Autosomal Dominant
craniometaphyseal dysplasia, autosomal dominant
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
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
- Craniometaphyseal Dysplasia, Autosomal Dominant
- Standard Disease Name
- craniometaphyseal dysplasia, autosomal dominant
- MeSH Tree
- No data
- ICD-10
- G93.6
Identifiers
- DO ID
- No data
- MeSH ID
- D001929
- OMIM ID
- MTHU007048
- UMLS ID
- C0006114
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:Excessive accumulation of fluid in the intracellular and/or extracellular spaces of the brain.|NCI2016_CTCAE_1602D:A disorder characterized by swelling due to an excessive accumulation of fluid in the brain.|NCI2016_02D:Swelling due to an excessive accumulation of fluid in the brain.|HPO2016_07_04:Abnormal accumulation of fluid in the brain. [HPO:curators]
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Herbs
target disease -> ingredient target -> herb ingredient8 Herbs
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