Phenotypes for disease #01803 (GM1G2 (gangliosidosis, GM1, type II), OMIM:230600)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000066771 - - - Familial, autosomal recessive 43y - 28y - - Ana Topf 00087249
0000232862 HP:0000708 Behavioral abnormality HP:0001288 Gait disturbance HP:0001263 Global developmental delay HP:0001249 Intellectual disability HP:0002344 Progressive neurologic deterioration - - Familial, autosomal recessive - 04y 03y - - Sarah Snanoudj 00307037
0000268942 HP:0001249; HP:0012751; HP:0001263; HP:0000750; HP:0002194; HP:0010862 - GM1-gangliosidosis, type II (OMIM 230500) Familial, autosomal recessive - - - - - Wenjuan Qiu 00373717
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