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cardiocranial syndrome, Pfeiffer type

Disease Summary
Associated Targets (0)

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Mondo Description Pfeiffer-type cardiocranial syndrome is an extremely rare disorder recognized in less than ten patients worldwide and characterized by a congenital heart defect, sagittal craniosynostosis and severe developmental delay (growth retardation and intellectual deficit).
Mondo Term and Equivalent IDs
MONDO:0009036:  cardiocranial syndrome, Pfeiffer type
GARD:0008586: 
MESH:C535578: 
Orphanet:2872: 
SCTID:720606005: 
UMLS:C1857495: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found