Jalili syndrome

Summary

Jalili syndrome is a developmental defect during embryogenesis^[1]. It draws 94 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).^[2]

Key Facts

• Jalili syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Jalili syndrome's instance of is recorded as rare disease^[4].
• Jalili syndrome's instance of is recorded as class of disease^[5].
• Jalili syndrome is a type of cone dystrophy^[6].
• Jalili syndrome is a type of amelogenesis imperfecta^[7].
• Jalili syndrome is a type of rare genetic developmental defect during embryogenesis^[8].
• Jalili syndrome is a type of malformation syndrome with odontal and/or periodontal component^[9].
• Jalili syndrome is a type of autosomal recessive disease^[10].
• Jalili syndrome is a type of syndrome^[11].
• Jalili syndrome's ICD-9-CM is recorded as 520.5^[12].
• Jalili syndrome's ICD-9-CM is recorded as 362.75^[13].
• Jalili syndrome's genetic association is recorded as CNNM4^[14].
• Jalili syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1873^[15].
• Jalili syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111404^[16].
• Jalili syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111404^[17].

Why It Matters

Jalili syndrome draws 94 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).^[2] It is known by 8 alternative names across languages and contexts.^[18]