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Diseases

Cyclocephaly

cyclocephaly

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
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]