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Human Disease

cranioectodermal dysplasia

Term ID

DOID:0050577

Synonyms

Levin syndrome
Sensenbrenner syndrome

Definition

A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies. (2)

References

Ontology

Human Disease ( DOID:0050577 )

Relationships

is a type of: autosomal recessive disease syndrome

autosomal recessive disease syndrome Show first 5 Terms
has subtype: cranioectodermal dysplasia 1 cranioectodermal dysplasia 2 cranioectodermal dysplasia 3 cranioectodermal dysplasia 4

cranioectodermal dysplasia 1 cranioectodermal dysplasia 2 cranioectodermal dysplasia 3 cranioectodermal dysplasia 4 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models