Phenotypes for disease #01806 (GD1 (Gaucher disease, type I), OMIM:230800)

27 entries on 1 page. Showing entries 1 - 27.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000325369 Splenomegaly, three asymptomatic; most very mild - - Unknown - - - - - Jimena Urbano 00435164
0000325371 I.13: splenomegaly, hepatomegaly, thrombocytopenia, cystalgia. I.30: splenomegaly, thrombocytopenia, leukopenia, chronic diarrhea, skin pigmentation. I.31:splenomegaly, hepatomegaly, thrombocytopenia, thrombocytopenia, leukopenia, stature and pubertal developmentdelayed, portal hypertension, irregularity of right humerus - GD1 Unknown - - - - - Jimena Urbano 00435166
0000325388 All splenomegaly, 6 patients also hepatomegaly, 7 patients with pancytopenia, 4with bone disease, one (I.39) asymptomatic at present age of 05y - GD1 Unknown - - - - - Jimena Urbano 00435165
0000325389 Both: splenomegaly, hepatomegaly, epistaxis. I.8: pancytopenia, femur deformity. I.24: thrombocytopenia - GD1 Unknown - - - - - Jimena Urbano 00435184
0000325390 splenomegaly - GD1 Unknown 07y - - - - Jimena Urbano 00435185
0000325391 splenomegaly, hepatomegaly, macrocephaly - GD1 Unknown 09y - - - - Jimena Urbano 00435186
0000325392 splenomegaly, thrombocytopenia, anemia, bone pain - GD1 Unknown 15y - - - - Jimena Urbano 00435187
0000325393 splenomegaly, hepatomegaly, thrombocytopenia - GD1 Unknown 10y - - - - Jimena Urbano 00435188
0000325394 splenomegaly, hepatomegaly, leukopenia, splenectomy at 9 yr - GD1 Unknown 09y - - - - Jimena Urbano 00435189
0000325395 splenomegaly, hepatomegaly, epistaxis, easy bruising, femur deformity, conjunctival pingueculae - GD1 Unknown 35y - - - - Jimena Urbano 00435190
0000325396 splenomegaly, hepatomegaly, femur infarcts - GD1 Unknown 05y - - - - Jimena Urbano 00435191
0000325398 Atypical parkinson - GD1 Unknown 47y - - - - Jimena Urbano 00435193
0000325399 splenomegaly, hepatomegaly, digestive hemorrhagia, ulcus gastroduodenal, hepatopathy, skin pigmentation, bone deformities - GD1 Unknown 39y - - - - Jimena Urbano 00435194
0000325400 splenomegaly, hepatomegaly, mild pancytopenia, epistaxis, bone crisis, femur deformity, skin pigmentation - GD1 Unknown 04y - - - - Jimena Urbano 00435195
0000325401 splenomegaly, hepatomegaly, anemia, bone disease - GD1 Unknown 04y - 00y07m - - Jimena Urbano 00435196
0000325402 splenomegaly, pancytopenia, bone deformity, aseptic necrosis - GD1 Unknown 25y - - - - Jimena Urbano 00435197
0000325403 splenomegaly, hepatomegaly, anemia, thrombocytopenia, stature development delayed, jaundice, skin pigmentation - GD1 Unknown 36y - 08y - - Jimena Urbano 00435199
0000325404 splenomegaly, thrombocytopenia, familial factor IX deficiency - GD1 Unknown 26y - - - - Jimena Urbano 00435200
0000325406 splenomegaly, hepatomegaly, pancytopenia - GD1 Unknown 06y - - - - Jimena Urbano 00435204
0000325407 splenomegaly, hepatomegaly, epistaxis, pancytopenia - GD1 Unknown 87y - - - - Jimena Urbano 00435205
0000325408 splenomegaly, hepatomegaly Gaucher disease GD1 Familial, autosomal recessive 14y - 02y06m - - Jimena Urbano 00435206
0000329989 see paper; ..., 5y-deceased (pulmonary complication); severe visceral involvement Gaucher disease GD1 Familial, autosomal recessive 05y - - - - Johan den Dunnen 00440091
0000329990 see paper; ..., moderate splenomegaly Gaucher disease GD1 Familial, autosomal recessive - - - - - Johan den Dunnen 00440092
0000329991 see paper; ..., severe bone disease Gaucher disease GD1 Familial, autosomal recessive - - - - - Johan den Dunnen 00440093
0000329992 see paper; ..., mild splenomegaly Gaucher disease GD1 Familial, autosomal recessive - - - - - Johan den Dunnen 00440094
0000329993 see paper; ..., severe splenomegaly Gaucher disease GD1 Familial, autosomal recessive - - - - - Johan den Dunnen 00440095
0000330008 see paper; ..., 9y-splenectomy; 10y-episodic bone pain, no fractures; 21y-massive hepatomegal, mild abnormalities function tests Gaucher disease GD1 Familial, autosomal recessive 21y 03y - - - Johan den Dunnen 00440110
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