Phenotypes for disease #04448 (CLN4B (lipofuscinosis, ceroid, neuronal, type 4, Parry type (CLN-4B)), OMIM:162350)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

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Individual ID     
0000066683 ceroid lipofuscinosis, neuronal, autosomal-dominant; granular osmiophilic deposits, curvilinear, fingerprint condensed - - Familial, autosomal dominant - - - - - Sara Mole 00087083
0000066684 ceroid lipofuscinosis, neuronal, autosomal-dominant - - Familial, autosomal dominant - - - - - Sara Mole 00087084
0000066685 diagnosed as Kufs; granular osmiophilic deposits - - Familial, autosomal dominant - - - - - Sara Mole 00087085
0000066686 see paper; ..., ceroid lipofuscinosis, neuronal, autosomal-dominant; myoclonic epilepsy, generalized tonic-clonic seizures, progressive cognitive deterioration with depression; followed by progressive motor neurological symptoms; granular osmiophilic deposits - - Familial, autosomal dominant - - - - - Sara Mole 00087086
0000066687 diagnosed as Kufs - - Familial, autosomal dominant - - - - - Sara Mole 00087087
0000082615 see paper; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00104700
0000082616 see paper; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00104701
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