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

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     
0000325368 died at 8.5m; splenomegaly, hepatomegaly, thrombocytopenia, anemia, seizures, head retroflection, hyperreflexia Gaucher disease GD2 Unknown 00y08m15d - 00y01m - - Jimena Urbano 00435163
0000329994 see paper; ..., classic type 2 Gaucher disease GD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00440096
0000329996 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 severe Gaucher disease type II GD2 Familial, autosomal recessive 00y00m01d - - - - Johan den Dunnen 00440098
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