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Search Results for -
GLYCOGEN STORAGE DISEASE, TYPE IV
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Also searched for:
1,4,ALPHA-GLUCAN 6-ALPHA-GLUCOSYLTRANSFERASE DEFICIENCY
AMYLOPECTINOSIS
ANDERSEN DISEASE
ANDERSEN'S DISEASE
BRANCHER DEFICIENCY
BRANCHER DEFICIENCY GLYCOGEN STORAGE DISEASE
BRANCHING ENZYME DEFICIENCY
BRANCHING-TRANSFERASE DEFICIENCY GLYCOGENOSIS
CIRRHOSIS, FAMILIAL, WITH DEPOSITION OF ABNORMAL GLYCOGEN
DEFICIENCY OF 1,4-ALPHA-GLUCAN BRANCHING ENZYME
DEFICIENCY OF AMYLO-(1,4,6)-TRANSGLYCOSYLASE
DEFICIENCY OF BRANCHING ENZYME
GBE1 DEFICIENCY
GLYCOGEN BRANCHING ENZYME DEFICIENCY
GLYCOGEN STORAGE DISEASE IV
GLYCOGEN STORAGE DISEASE TYPE IV
GLYCOGENOSIS IV
GLYCOGENOSIS, TYPE 4
GSD IV
GSD4
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Repository:
NINDS Repository
(26580)
NIGMS Human Genetic Cell Repository
(5519)
NIA Aging Cell Culture Repository
(1281)
HD Community Biorepository
(76)
Centers for Disease Control and Prevention Repository
(27)
Orphan Disease Center
(13)
Allen Cell Collection
(2)
Autism
(2)
Collection:
Cerebrovascular Disease
(13886)
Parkinsonism
(6953)
Motor Neuron Disease
(5555)
Heritable Diseases
(5428)
Control
(937)
Lysosomal Storage Diseases
(753)
Apparently Healthy Collection
(486)
Muscular Dystrophies
(361)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(260)
Alzheimer's Disease
(252)
Venezuelan Huntington Disease
(251)
Dystonia
(247)
Chromosome Abnormalities
(245)
PIGI Consented Sample
(238)
Canadian Alzheimer Disease
(226)
Maturity-Onset Diabetes of the Young
(222)
Old Order Amish Major Affective Disorder
(212)
Hereditary Cancers
(162)
GeT-RM Samples
(160)
CMD Specific
(138)
Italian Alzheimer Disease
(121)
dbGaP
(112)
German Alzheimer Disease
(101)
Alzheimer Disease With No Family History
(31)
Disorders of the Urea Cycle
(17)
CEPH
(15)
Epilepsy
(12)
Pharmacogenetics
(11)
Whole-Genome Sequence
(11)
Animals
(10)
DGAP
(6)
Frontotemporal Degeneration
(6)
Specially Characterized Fibroblasts
(6)
GRC
(5)
Gene-Edited hiPSC
(5)
Engineered Cell Cultures
(4)
Human Variation
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Non-Healing Wound Collection
(4)
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(3)
Apparently healthy iPSCs
(3)
FOXG1
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DNA
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LCL
(10522)
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(1883)
iPSC
(85)
Plasmid
(64)
96 well plate of DNA samples
(33)
Melanocyte
(31)
Keratinocyte
(26)
Preprocessed DNA
(20)
High Molecular Weight DNA
(13)
Neuronally-derived
(12)
Amniotic fluid-derived cell line
(6)
Epithelial
(4)
Tumor-derived cell line
(2)
aging mapping panel
(2)
Chorionic villus-derived cell line
(1)
Microcell hybrid
(1)
Affected:
Yes
(28137)
No
(2677)
At Risk
(1552)
Unknown
(57)
Mutation Data Available:
N
(30366)
Y
(3099)
No
(35)
Source:
Whole Blood
(11515)
B-Lymphocyte
(10534)
LCL
(8785)
Fibroblast
(570)
Skin, Arm
(273)
Skin, Unspecified
(249)
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(83)
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(58)
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(33)
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(31)
Brain striatum
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(9)
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Breast organoid
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(3)
Umbilical Cord, Umbilical cord
(3)
Muscle, Unspecified
(2)
Skin, Abdomen
(2)
Skin, Leg
(2)
Spleen, Keloid
(2)
Amnion, Amnion
(1)
Blood
(1)
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(1)
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(1)
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(1)
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(1)
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(1)
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(1)
Cornea, Cornea
(1)
Epithelial
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Eye
(1)
Fetal, Unspecified
(1)
Gonad, Ovary
(1)
Heart, Pericardium
(1)
Heart, Unspecified
(1)
Hydatidiform mole
(1)
Kidney, Kidney
(1)
Lens, Eye
(1)
Placental, Placenta
(1)
Skin, Calf
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Skin, Fetal
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(1)
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(1)
Tumor-derived cell line
(1)
Umbilical Cord, Vein, umbilical
(1)
Sex:
Male
(16916)
Female
(16374)
Other
(9)
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White
(27513)
Black/African American
(3238)
Asian
(504)
Other
(436)
More than one race
(298)
Unknown
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American Indian/Alaska Native
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Native Hawaiian/Other Pacific Islander
(53)
Hispanic/Latino
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Not Reported
(39)
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Caucasian
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Korean
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Japanese
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Filipino
(2)
Chinese
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Vietnamese
(1)
dbGap Data Available:
No
(28504)
Yes
(4996)
Extended Clinical Data Available:
Yes
(26750)
No
(6750)
Age at Sampling (Years):
55-64
(7487)
65-74
(6253)
45-54
(6249)
75-89
(3779)
35-44
(3343)
25-34
(1761)
15-24
(1272)
5-14
(1247)
0-4
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90-99
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100+
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