01
- 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
- Congenital cerebral hernia
- Standard Disease Name
- congenital cerebral hernia
- MeSH Tree
- No data
- ICD-10
- Q01|Q01.9
Identifiers
- DO ID
- No data
- MeSH ID
- D004677
- OMIM ID
- MTHU002500|MTHU000609
- UMLS ID
- C0014065
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A congenital neural tube closure defect resulting in the protrusion of the brain through a skull opening. When the protrusion includes the meninges, the term encephalomeningocele is used.|MSH2017_2016_08_12:Brain tissue herniation through a congenital or acquired defect in the skull. The majority of congenital encephaloceles occur in the occipital or frontal regions. Clinical features include a protuberant mass that may be pulsatile. The quantity and location of protruding neural tissue determines the type and degree of neurologic deficit. Visual defects, psychomotor developmental delay, and persistent motor deficits frequently occur.|HPO2016_07_04:A neural tube defect characterized by sac-like protrusions of the brain and the membranes that cover it through openings in the skull. [HPO:probinson]|HPO2016_07_04:A congenital defect in the skull, whereby there is a protrusion of part of the cranial contents through a congenital defect in the cranium, usually covered with skin or mucous membrane. The term encephalocele refers to a subclass of these lesions in which brain tissue protrudes through the defect. [HPO:probinson] {name="PMID:24931720"}
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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