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

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

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Age/Diagnosis     

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Individual ID     
0000233297 Global developmental delay, Seizures, Abnormal facial shape - - Familial, autosomal recessive - 02y02m 00y01m - - Corina-Marcela Rus 00307873
0000257301 Neuroregression, myoclonic epilepsy - - Familial, autosomal recessive - - - - - Anju Shukla 00361905
0000337691 Global developmental delay, Intellectual disability, Cerebral palsy, Seizure, Myoclonic seizures, Delayed speech and language development - - Familial, autosomal recessive 12y - - - - Andreas Laner 00448514
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