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Search Results for -
GLYCOGENOSIS, TYPE 5
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GLYCOGEN STORAGE DISEASE TYPE V
GLYCOGEN STORAGE DISEASE V
GLYCOGEN STORAGE DISEASE, TYPE V
GSD V
GSD5
MCARDLE DISEASE
MCARDLE'S DISEASE
MUSCLE GLYCOGEN PHOSPHORYLASE DEFICIENCY
MYOPHOSPHORYLASE DEFICIENCY
MYOPHOSPHORYLASE DEFICIENCY GLYCOGENOSIS
PYGM DEFICIENCY
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Repository:
NINDS Repository
(9718)
NIGMS Human Genetic Cell Repository
(9482)
NIA Aging Cell Culture Repository
(1580)
NHGRI Sample Repository for Human Genetic Research
(954)
Autism
(164)
HD Community Biorepository
(36)
Orphan Disease Center
(13)
Centers for Disease Control and Prevention Repository
(12)
Allen Cell Collection
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Heritable Diseases
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Motor Neuron Disease
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Cerebrovascular Disease
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Epilepsy
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Tourette Syndrome
(1470)
Chromosome Abnormalities
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NHGRI Sample Repository for Human Genetic Research
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Apparently Healthy Collection
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Lysosomal Storage Diseases
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PIGI Consented Sample
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dbGaP
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Human Variation
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CEPH
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Muscular Dystrophies
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Control
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Parkinsonism
(297)
GeT-RM Samples
(289)
Dystonia
(278)
Old Order Amish Major Affective Disorder
(272)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(260)
Animals
(241)
Hereditary Cancers
(240)
Repository Linkage Families
(228)
Canadian Alzheimer Disease
(226)
Maturity-Onset Diabetes of the Young
(222)
CMD Specific
(175)
GRC
(131)
Disorders of the Urea Cycle
(121)
Pharmacogenetics
(113)
University of Georgia Centenarian Study
(80)
Alzheimer's Disease
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Retinitis Pigmentosa Foundation Collection
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Nonhuman Primates
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Venezuelan Huntington Disease
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The 90+ Study
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DGAP
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FOXG1
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Italian Alzheimer Disease
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German Alzheimer Disease
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Ames Dwarf Mice
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Aged Sib Pairs
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Specially Characterized Fibroblasts
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Engineered Cell Cultures
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Whole-Genome Sequence
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Gene-Edited hiPSC
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Stem Cell Collection
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Alzheimer Disease With No Family History
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Apparently healthy iPSCs
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Non-Healing Wound Collection
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DNA
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LCL
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Somatic cell hybrid
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iPSC
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Endothelial
(39)
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High Molecular Weight DNA
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mESC
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FFPE
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Mesothelial
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Microcell hybrid
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Neuronally-derived
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Protein
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hybrid regional mapping panel
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Affected:
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No
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At Risk
(303)
Unknown
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Mutation Data Available:
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Y
(3442)
No
(1)
Source:
B-Lymphocyte
(7725)
LCL
(5589)
Whole Blood
(4174)
Fibroblast
(947)
Skin, Arm
(395)
Skin, Unspecified
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Somatic cell hybrid
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Skin, Skin
(136)
Lung, Lung
(94)
Skin, Foreskin
(69)
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(44)
Aorta, thoracic
(40)
Amniotic fluid
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Skin, Ear
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Fetal, Unspecified
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Blood
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Skin, Posterior iliac crest
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Skin, Thorax
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Artery, iliac
(7)
Artery, pulmonary
(7)
Skin, Buttock
(7)
Skin, Sacrum
(7)
Skin, Thorax/abdomen
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Gonad, Ovary
(6)
Skin, Back
(6)
Skin, Inguinal area
(6)
Skin, Buttock-thigh
(5)
Skin, Leg
(5)
Whole embryo, Embryo
(5)
Breast organoid
(4)
Chorionic villus
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Gonad, Gonad
(4)
Skin, Hip
(4)
Stem cell
(4)
Chorionic villus-derived cell line
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Eye
(3)
Muscle, Unspecified
(3)
Umbilical Cord, Umbilical cord
(3)
Aorta, abdominal
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Conjunctiva, Conjunctiva
(2)
Embryonal carcinoma
(2)
Gingival, Gum
(2)
Kidney, Kidney
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Liver, Liver
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Placental, Placenta
(2)
Skin, Fetal
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Skin, Genital area
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Skin, Labialscrotal fold
(2)
Skin, Thoraco-lumbar junction
(2)
Skin, Toe
(2)
Skin, Umbilical area
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T-Lymphocyte
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Tendon, Achilles tendon
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Trachealis muscle
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Vein, umbilical
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Adenocarcinoma
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Amnion, Amnion
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Artery, Aorta, thoracic
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Artery, carotid
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Ascites fluid, Ascites fluid
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Bladder carcinoma
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Brain striatum
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Brain, Brain
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Cartilage, Nasal
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Cartilage, Unspecified
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Cornea, Cornea
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Endometrial, Uterus
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Endothelial
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Epithelial
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Ewing sarcoma
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Fetal, Arm
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Gonad, Testes
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Heart, Pericardium
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Heart, Unspecified
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Kidney
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Lens, Eye
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Lung
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Polyp, Nasal
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Skin, Calf
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Smooth muscle
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Tumor
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Tumor, Neurofibroma
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Tumor-derived cell line
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Umbilical Cord, Vein, umbilical
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Uterine muscle, Uterus
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Sex:
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(11204)
Female
(10146)
Other
(17)
Race:
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Black/African American
(1043)
More than one race
(458)
Asian
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Other
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Chinese
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East Indian
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Not Reported
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Asian, Other
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Native Hawaiian/Other Pacific Islander
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Filipino
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Korean
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Japanese
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Vietnamese
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dbGap Data Available:
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(19133)
Yes
(2829)
Extended Clinical Data Available:
No
(11865)
Yes
(10097)
Age at Sampling (Years):
5-14
(5905)
55-64
(2225)
45-54
(2074)
35-44
(1806)
0-4
(1672)
65-74
(1660)
25-34
(1563)
15-24
(1351)
75-89
(836)
90-99
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100+
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