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Jalili syndrome

Disease Summary
Associated Targets (2)
Tbio

1

Tdark

1


GARD Rare
Mondo Description Jalili syndrome is characterized by the association of amelogenesis imperfecta (AI) and cone-rod retinal dystrophy (CORD).
Uniprot Description A syndrome characterized by the association of cone-rod dystrophy and amelogenesis imperfecta.
Mondo Term and Equivalent IDs
MONDO:0009007:  Jalili syndrome
DOID:0111404: 
GARD:0001463: 
MESH:C000596385: 
Orphanet:1873: 
SCTID:707608003: 
UMLS:C3495589: 
UMLS:CN200616: