ZFIN Human Disease: cranioectodermal dysplasia

OBO ID: DOID:0050577

Term Name:	cranioectodermal dysplasia		Search Ontology:
Synonyms:	Levin syndrome Sensenbrenner syndrome
Definition:	A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies. (2)
References:	MESH:C562966 OMIM:PS218330
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

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None