progressive myoclonic epilepsy type 3

Summary

progressive myoclonic epilepsy type 3 is a class of disease^[1].

Key Facts

• progressive myoclonic epilepsy type 3's instance of is recorded as class of disease^[2].
• progressive myoclonic epilepsy type 3's subclass of is recorded as neuronal ceroid lipofuscinosis^[3].
• progressive myoclonic epilepsy type 3's OMIM ID is recorded as 611726^[4].
• progressive myoclonic epilepsy type 3's Orphanet ID is recorded as 263516^[5].
• progressive myoclonic epilepsy type 3's genetic association is recorded as KCTD7^[6].
• progressive myoclonic epilepsy type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_263516^[7].
• progressive myoclonic epilepsy type 3's UMLS CUI is recorded as C2673257^[8].
• progressive myoclonic epilepsy type 3's ICD-10-CM is recorded as G40.3^[9].
• progressive myoclonic epilepsy type 3's GARD rare disease ID is recorded as 2167^[10].
• progressive myoclonic epilepsy type 3's Mondo ID is recorded as MONDO_0012721^[11].
• progressive myoclonic epilepsy type 3's UniProt disease ID is recorded as DI-00955^[12].