Phenotypes for disease #02062 (Sandhoff (Sandhoff disease), OMIM:268800)

19 entries on 1 page. Showing entries 1 - 19.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060503 Sandhoff disease, infantile, juvenile, and adult forms (OMIM:268800) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080934
0000060584 Sandhoff disease, infantile, juvenile, and adult forms (OMIM:268800) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081015
0000104385 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132191
0000104386 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132192
0000104387 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132193
0000104388 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132194
0000104389 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132195
0000104390 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132196
0000104391 juvenile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132197
0000104392 infantile - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132198
0000104393 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132200
0000104394 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132201
0000104395 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132202
0000104396 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132203
0000104397 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132204
0000104398 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132205
0000104399 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00132206
0000258101 HP:0010729 Cherry red spot of the macula HP:0001324 Muscle weakness HP:0001250 Seizure HP:0002333 Motor deterioration - SANDHOFF Familial, autosomal recessive - - - Sandhoff Disease ORPHA:796 - Massoud Houshmand 00362731
0000342143 juvenile Sandhoff disease Sandhoff disease Sandhoff disease Unknown - - - - - Johan den Dunnen 00453481
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