L1 syndrome

Summary

L1 syndrome is a class of disease^[1]. It draws 5 Wikipedia views per month (class_of_disease category, ranking #627 of 1,968).^[2]

Key Facts

• L1 syndrome's instance of is recorded as class of disease^[3].
• L1 syndrome's subclass of is recorded as syndrome with corpus callosum agenesis /dysgenesis as a major feature^[4].
• L1 syndrome's Orphanet ID is recorded as 275543^[5].
• L1 syndrome's genetic association is recorded as L1CAM^[6].
• L1 syndrome's Google Knowledge Graph ID is recorded as /g/11fk53rt9w^[7].
• L1 syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_275543^[8].
• L1 syndrome's ICD-10-CM is recorded as Q04.8^[9].
• L1 syndrome's GARD rare disease ID is recorded as 12524^[10].
• L1 syndrome's Mondo ID is recorded as MONDO_0017140^[11].
• L1 syndrome's Genetics Home Reference Conditions ID is recorded as l1-syndrome^[12].

Why It Matters

L1 syndrome draws 5 Wikipedia views per month (class_of_disease category, ranking #627 of 1,968).^[2]