Jalili syndrome is characterized by the association of amelogenesis imperfecta (AI) and cone-rod retinal dystrophy (CORD).
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
inherited bleeding disorder, platelet-type
MONDO:0000009
infantile liver failure
MONDO:0000023
febrile seizures, familial
MONDO:0000032
hereditary hypophosphatemic rickets
MONDO:0000044
hypothyroidism, congenital, nongoitrous
MONDO:0000045
isolated microphthalmia
MONDO:0000062