DOID:1686
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Homo sapiens (human)
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DOID:3068
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-
glioblastoma
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Aliases:
-
GBM
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adult glioblastoma multiforme
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glioblastoma multiforme
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grade IV adult Astrocytic tumor
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primary glioblastoma multiforme
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spongioblastoma multiforme
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|
|
Homo sapiens (human)
|
DOID:6128
|
-
gliomatosis cerebri
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Aliases:
|
|
|
Homo sapiens (human)
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DOID:3071
|
-
gliosarcoma
-
Aliases:
-
Glioblastoma with sarcomatous component
|
|
|
Homo sapiens (human)
|
DOID:2436
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|
|
|
Homo sapiens (human)
|
DOID:2921
|
|
|
|
Homo sapiens (human)
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DOID:0050851
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|
|
|
Homo sapiens (human)
|
DOID:2431
|
-
glomus tumor
-
Aliases:
-
Glomus neoplasm
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Glomus tumour
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|
|
Homo sapiens (human)
|
DOID:14080
|
-
glucocorticoid-remediable aldosteronism
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Aliases:
-
GRA
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GRS
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familial hyperaldosteronism type I
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glucocorticoid-suppressible hyperaldosteronism
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|
|
Homo sapiens (human)
|
DOID:10603
|
-
glucose intolerance
-
Aliases:
-
Glucose malabsorption
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Malabsorption of glucose
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|
|
Homo sapiens (human)
|
DOID:4194
|
-
glucose metabolism disease
-
Aliases:
-
disorder of glucose metabolism
|
|
|
Homo sapiens (human)
|
DOID:2862
|
-
glucosephosphate dehydrogenase deficiency
-
Aliases:
-
Glucose-6-phosphate dehydrogenase deficiency
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deficiency of G-6PD
|
|
|
Homo sapiens (human)
|
DOID:0111681
|
-
glutamate-cysteine ligase deficiency
-
Aliases:
-
gamma-glutamylcysteine synthetase deficiency
-
hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111254
|
-
glutaric acidemia I
-
Aliases:
-
GA1
-
glutaric academia type 1
-
glutaric aciduria 1
-
glutaric aciduria type I
-
glutaryl-coA dehydrogenase deficiency
-
glutaryl-coenzyme A dehydrogenase deficiency
|
|
|
Homo sapiens (human)
|
DOID:0060363
|
-
glycerol kinase deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111037
|
-
glycine N-methyltransferase deficiency
-
Aliases:
-
GNMT deficiency
-
hypermethioninemia due to GNMT deficiency
-
hypermethioninemia due to glycine N-methyltransferase deficiency
|
|
|
Homo sapiens (human)
|
DOID:9268
|
-
glycine encephalopathy
-
Aliases:
-
Non-ketotic hyperglycinemia
-
nonketotic hyperglycinemia
|
|
|
Homo sapiens (human)
|
DOID:2752
|
-
glycogen storage disease II
-
Aliases:
-
Generalized glycogenosis
-
Glycogen storage disease 2
-
Glycogen storage disease, type II
-
Glycogenosis, type 2
-
Lysosomal alpha-1,4-glucosidase deficiency
-
Pompe's disease
-
acid maltase deficiency
-
deficiency of glucoamylase
-
deficiency of maltase
-
glycogen storage disease type II
|
|
|
Homo sapiens (human)
|
DOID:2748
|
-
glycogen storage disease III
-
Aliases:
-
Glycogen storage disease 3
-
Glycogen storage disease, type III
-
amylo 1,6 glucosidase deficiency
-
deficiency of debranching enzyme
-
deficiency of dextrin
|
|
|
Homo sapiens (human)
|
DOID:2750
|
-
glycogen storage disease IV
-
Aliases:
-
Amylopectinosis
-
Branching-transferase deficiency glycogenosis
-
Glycogen storage disease 4
-
Glycogen storage disease, type IV
-
brancher deficiency glycogenosis
-
deficiency of 1,4-alpha-glucan branching enzyme
|
|
|
Homo sapiens (human)
|
DOID:0111042
|
-
glycogen storage disease IXa
-
Aliases:
-
GSD type 9A
-
GSD type IXa
-
GSD9A
-
glycogen storage disease type 9A
-
glycogen storage disease type IXa
-
glycogenosis type 9A
-
glycogenosis type IXa
|
|
|
Homo sapiens (human)
|
DOID:0111041
|
-
glycogen storage disease IXb
-
Aliases:
-
GSD IXb
-
GSD due to liver and muscle phosphorylase kinase deficiency
-
GSD type 9B
-
GSD type IXb
-
GSD9B
-
glycogen storage disease type 9B
-
glycogen storage disease type IXb
-
glycogenosis due to liver and muscle phosphorylase kinase deficiency
-
glycogenosis type 9B
-
glycogenosis type IXb
|
|
|
Homo sapiens (human)
|
DOID:0111043
|
-
glycogen storage disease IXc
-
Aliases:
-
GSD type 9C
-
GSD type IXc
-
GSD9C
-
glycogen storage disease type 9C
-
glycogen storage disease type IXc
-
glycogenosis type 9C
-
glycogenosis type IXc
|
|
|
Homo sapiens (human)
|
DOID:0111040
|
-
glycogen storage disease IXd
-
Aliases:
-
GSD IXd
-
GSD due to muscle phosphorylase kinase deficiency
-
GSD type 9D
-
GSD type 9E
-
GSD type IXd
-
GSD type IXe
-
GSD9D
-
X-linked muscke glycogenosis
-
glycogen storage disease due to muscle phosphorylase kinase deficiency
-
glycogen storage disease type 9D
-
glycogen storage disease type 9E
-
glycogen storage disease type IXd
-
glycogen storage disease type IXe
-
glycogenosis due to muscle phosphorylase kinase deficiency
-
glycogenosis type 9D
-
glycogenosis type 9E
-
glycogenosis type IXd
-
glycogenosis type IXe
-
muscle phosphorylase kinase deficiency
|
|
|
Homo sapiens (human)
|
DOID:2749
|
-
glycogen storage disease Ia
|
|
|
Homo sapiens (human)
|