Phenotypes for disease #01804 (GM1G3 (gangliosidosis, GM1 type III), OMIM:230650)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000232562 HP:0007256 Abnormal pyramidal sign HP:0001290 Generalized hypotonia HP:0001263 Global developmental delay HP:0001249 Intellectual disability HP:0007153 Progressive extrapyramidal movement disorder - - Familial, autosomal recessive - 06y 05y - - Sarah Snanoudj 00306728
0000232913 - - - Familial, autosomal recessive - 04y 04y - - Sarah Snanoudj 00307107
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