Disease #01807 (GD2 (Gaucher disease, type II), OMIM:230900)

Official abbreviation GD2
Name Gaucher disease, type II
OMIM ID 230900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene GBA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-06-13 22:17:21 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00435163 PatII.1 PubMed: Cormand 1998 - ? - Spain - 00y08m15d - - - GD2 died at 8.5m; splenomegaly, hepatomegaly, thrombocytopenia, anemia, seizures, head retroflection, hyperreflexia GBA GBA 1 1 Jimena Urbano
00440096 MSM82 PubMed: Latham 1991 - - - United States white - - - - GD2 see paper; ..., classic type 2 GBA GBA 2 1 Johan den Dunnen
00440098 patient PubMed: Uchiyama 1994 - F - Japan - 00y00m01d - - - GD2 see paper; ..., 37w-birth Caesarean section due to fetal distress; 9h-deceased; severe asphyxia, respiration did not become voluntary; autopsy hepatomegaly, no activity of glucocerebrosidase GBA GBA 2 1 Johan den Dunnen
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