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Pai syndrome

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description Pai syndrome is an idiopathic developmental disorder characterized by median cleft of the upper lip (MCL), midline polyps of the facial skin and nasal mucosa, and pericallosal lipomas. Hypertelorism with ocular anomalies are also observed, generally with normal neuropsychological development.
Mondo Term and Equivalent IDs
MONDO:0007956:  Pai syndrome
GARD:0003439: 
MESH:C536135: 
Orphanet:1993: 
SCTID:722201004: 
UMLS:C1835087: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found