Disease #01804 (GM1G3 (gangliosidosis, GM1 type III), OMIM:230650)

Official abbreviation GM1G3
Name gangliosidosis, GM1 type III
OMIM ID 230650
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 2
Associated with 1 gene GLB1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-03-17 08:51:38 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00245727 - PubMed: Higaki et al 2011 - - - - Japanese - - - - GM1G3 - GLB1 GLB1 2 1 LOVD
00245728 - PubMed: Higaki et al 2011 - - - - - - - - - GM1G3 - GLB1 GLB1 2 1 LOVD
00245737 - PubMed: Higaki et al 2011 - - - - - - - - - GM1G3 - GLB1 GLB1 2 1 LOVD
00245738 - PubMed: Higaki et al 2011 - - - - Japanese - - - - GM1G3 - GLB1 GLB1 2 1 LOVD
00245740 - PubMed: Higaki et al 2011 - - - - Belgian - - - - GM1G3 - GLB1 GLB1 2 1 LOVD
00306728 - - - M no - - - - - - GM1G3 HP:0007256 Abnormal pyramidal sign HP:0001290 Generalized hypotonia HP:0001263 Global developmental delay HP:0001249 Intellectual disability HP:0007153 Progressive extrapyramidal movement disorder GLB1 GLB1 2 1 Sarah Snanoudj
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