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Neuronal ceroid lipofuscinosis
- ... the condition. Cathepsin D deficiency Cathepsin D deficient neuronal ceroid lipofuscinosis CLN10 Congenital neuronal ceroid lipofuscinosis Neuronal ceroid lipofuscinosis ...
- ... of the condition. CLN1 Infantile Batten disease Infantile neuronal ceroid lipofuscinosis Neuronal ceroid lipofuscinosis 1 Neuronal ceroid lipofuscinosis, infantile ...
- ... Bielschowsky disease Late-infantile Batten disease Late-infantile neuronal ceroid lipofuscinosis LINCL Neuronal ceroid lipofuscinosis, late-infantile Genetic Testing ...
- ... not show signs and symptoms of the condition. Neuronal ceroid lipofuscinosis 8 Genetic Testing Registry: Neuronal ceroid lipofuscinosis 8 northern epilepsy variant Genetic Testing Registry: Neuronal ...
- ... history of the disorder in their family. Adult neuronal ceroid lipofuscinosis Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant CLN4B Parry ... Registry: Ceroid lipofuscinosis, neuronal, 4 (Kufs type) Adult neuronal ceroid lipofuscinosis ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
- ... symptoms of the condition. Finnish variant late infantile neuronal ceroid lipofuscinosis Finnish vLINCL Jansky-Bielschowsky disease Late-infantile neuronal ...
- ... condition. CLN7 CLN7 disease, late infantile MFSD8-related neuronal ceroid lipofuscinosis Genetic Testing Registry: Neuronal ceroid lipofuscinosis 7 CLN7 ...
- ... Mayou disease Batten-Spielmeyer-Vogt disease CLN3-related neuronal ceroid-lipofuscinosis Juvenile Batten disease Juvenile cerebroretinal degeneration Juvenile neuronal ...
- ... the condition. Ceroid lipofuscinosis neuronal 6 CLN6-related neuronal ceroid lipofuscinosis Neuronal ceroid lipofuscinosis 6 Genetic Testing Registry: Ceroid ...
- ... lobar degeneration. Ceroid lipofuscinosis, neuronal, 11 GRN-related neuronal ceroid-lipofuscinosis Genetic Testing Registry: Neuronal ceroid lipofuscinosis 11 National ...