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Search Results for -
DEFICIENCY OF ALPHA-GALACTOSIDASE
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ALPHA-GALACTOSIDASE A DEFICIENCY
ALPHA-GALACTOSIDASE-A DEFICIENCY
ANDERSON-FABRY DISEASE
ANGIOKERATOMA CORPORIS DIFFUSUM
ANGIOKERATOMA CORPORIS DIFFUSUM UNIVERSALE
CARDIOVASORENAL SYNDROME
CERAMIDE LACTOSIDE LIPIDOSIS
CERAMIDE TRIHEXOSIDASE DEFICIENCY
DEFICIENCY OF MELIBIASE
FABRY DISEASE
FABRY'S DISEASE
GLA DEFICIENCY
HEREDITARY DYSTOPIC LIPIDOSIS
LACTOSYL CERAMIDOSIS
RUITER-POMPEN SYNDROME
SWEELEY-KLIONSKY DISEASE
THESAURISMOSIS HEREDITARIA
THESAURISMOSIS LIPOIDICA
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NIGMS Human Genetic Cell Repository
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NHGRI Sample Repository for Human Genetic Research
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Old Order Amish Major Affective Disorder
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University of Georgia Centenarian Study
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The 90+ Study
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"Intra-abdominal fat and risk of disease in children and adolescents" study
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Venezuelan Huntington Disease
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Alzheimer's Disease
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CMD Specific
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Pharmacogenetics
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Canadian Alzheimer Disease
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Disorders of the Urea Cycle
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Maturity-Onset Diabetes of the Young
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CEPH
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Retinitis Pigmentosa Foundation Collection
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FOXG1
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96 well plate of DNA samples
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human variation panel
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aging mapping panel
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FFPE
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gene mutation panel
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No
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LCL
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Whole Blood
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Blood
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Stem cell
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Vein, iliac
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Amniotic fluid-derived cell line
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Skin, Leg
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Whole embryo, Embryo
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Skin, Posterior iliac crest
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Breast organoid
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Muscle, Unspecified
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Skin, Back
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Umbilical Cord, Umbilical cord
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Conjunctiva, Conjunctiva
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Epithelial
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dbGap Data Available:
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Extended Clinical Data Available:
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45-54
(2650)
25-34
(2542)
15-24
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(2197)
5-14
(2107)
0-4
(1971)
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75-89
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100+
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