Disease #03049 (EPM3;CLN14 (epilepsy, myoclonic, progressive, type 3 (EPM-3, neuronal ceroid lipofuscinosis, type 14 (CLN-14))), OMIM:611726)

Official abbreviation EPM3;CLN14
Name epilepsy, myoclonic, progressive, type 3 (EPM-3, neuronal ceroid lipofuscinosis, type 14 (CLN-14))
OMIM ID 611726
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene KCTD7
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00307873 ? - - F yes Saudi Arabia - - - - - EPM3;CLN14 Global developmental delay, Seizures, Abnormal facial shape KCTD7 KCTD7 1 1 Corina-Marcela Rus
00361905 - - - - - - - - - - - EPM3;CLN14, FMFD Neuroregression, myoclonic epilepsy - KCTD7, MEFV 2 1 Anju Shukla
00448514 284164 - - F yes Saudi Arabia - - - - - EPM3;CLN14 Global developmental delay, Intellectual disability, Cerebral palsy, Seizure, Myoclonic seizures, Delayed speech and language development KCTD7 KCTD7 1 1 Andreas Laner
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