01
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Cyclocephaly
- Standard Disease Name
- cyclocephaly
- MeSH Tree
- No data
- ICD-10
- Q87.0
Identifiers
- DO ID
- No data
- MeSH ID
- C562573
- OMIM ID
- MTHU026547|236100|MTHU014657
- UMLS ID
- C0266667
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:The most severe form of holoprosencephaly in which there is a complete absence of midline forebrain division resulting in the presence of fused hemispheres and a single ventricle (alobar holoprosencephaly). It is mapped to chromosome 21q22.|HPO2016_07_04:Cyclopia is a congenital abnormality in which there is only one eye. That eye is centrally placed in the area normally occupied by the root of the nose. [DDD:ncarter]
Related
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Related Targets
target disease8 Targets