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Search Results for -
ATAXIA TELANGIECTASIA
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AT
AT1
ATA
ATAXIA TELANGIECTASIA SYNDROME
ATAXIA-TELANGIECTASIA
ATAXIA-TELANGIECTASIA SYNDROME
ATAXIA-TELANGIECTASIA VARIANT V1
ATC
ATD
ATE
AT-V1
AT-V2
BBS
IMMUNODEFICIENCY, MICROCEPHALY, AND CHROMOSOMAL INSTABILITY
LOUIS-BAR SYNDROME
MICROCEPHALY WITH NORMAL INTELLIGENCE, IMMUNODEFICIENCY, AND LYMPHORETICULAR MALIGNANCIES
MICROCEPHALY, NORMAL INTELLIGENCE AND IMMUNODEFICIENCY
NBS
NBS - NIJMEGEN BREAKAGE SYNDROME
NIJMEGEN BREAKAGE SYNDROME
NONSYNDROMAL MICROCEPHALY, AUTOSOMAL RECESSIVE, WITH NORMAL INTELLIGENCE
SEEMANOVA SYNDROME II
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Repository:
NINDS Repository
(12720)
NIGMS Human Genetic Cell Repository
(5849)
NHGRI Sample Repository for Human Genetic Research
(4940)
AREDS2
(1889)
NIA Aging Cell Culture Repository
(899)
Allen Cell Collection
(57)
HD Community Biorepository
(32)
Centers for Disease Control and Prevention Repository
(22)
Autism
(8)
Orphan Disease Center
(6)
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Heritable Diseases
(5289)
Cerebrovascular Disease
(5195)
NHGRI Sample Repository for Human Genetic Research
(4940)
Epilepsy
(2630)
Control
(1553)
Parkinsonism
(1446)
Tourette Syndrome
(1352)
Chromosome Abnormalities
(743)
Motor Neuron Disease
(514)
Lysosomal Storage Diseases
(431)
PIGI Consented Sample
(378)
Muscular Dystrophies
(304)
GeT-RM Samples
(273)
Hereditary Cancers
(270)
Dystonia
(223)
Hybrids
(203)
Old Order Amish Major Affective Disorder
(198)
dbGaP
(188)
Canadian Alzheimer Disease
(173)
CMD Specific
(163)
Apparently Healthy Collection
(159)
Retinitis Pigmentosa Foundation Collection
(154)
Venezuelan Huntington Disease
(151)
Disorders of the Urea Cycle
(146)
Alzheimer's Disease
(116)
Animals
(96)
Pharmacogenetics
(96)
CEPH
(93)
Italian Alzheimer Disease
(92)
Maturity-Onset Diabetes of the Young
(82)
German Alzheimer Disease
(80)
Human Variation
(64)
Ames Dwarf Mice
(47)
Repository Linkage Families
(43)
FOXG1
(29)
GRC
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DGAP
(18)
Alzheimer Disease With No Family History
(14)
Specially Characterized Fibroblasts
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Nonhuman Primates
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Aged Sib Pairs
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Cardiomyopathy
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Non-Healing Wound Collection
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Whole-Genome Sequence
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Gene-Edited hiPSC
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Prostate Cancer
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Apparently healthy iPSCs
(2)
Frontotemporal Degeneration
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Engineered Cell Cultures
(1)
Laminopathy
(1)
Skeletal Myopathy
(1)
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DNA
(16944)
LCL
(7359)
Fibroblast
(1711)
Somatic cell hybrid
(140)
iPSC
(128)
Plasmid
(29)
High Molecular Weight DNA
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Smooth muscle
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Adipose stromal cell
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Endothelial
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Amniotic fluid-derived cell line
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Neuronally-derived
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Antibodies
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FFPE
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Keratinocyte
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Microcell hybrid
(1)
Affected:
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(11743)
At Risk
(6121)
Unknown
(2514)
No
(2402)
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(22548)
Y
(3866)
No
(8)
Source:
Whole Blood
(8891)
B-Lymphocyte
(7378)
LCL
(5868)
Fibroblast
(565)
Skin, Arm
(267)
Skin, Unspecified
(265)
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(110)
Somatic cell hybrid
(63)
Stem cell
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Skin, Ear
(49)
Skin, Thigh
(32)
Aorta, thoracic
(16)
Lung, Lung
(14)
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(12)
Amniotic fluid
(11)
Trachealis muscle
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(8)
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Blood
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Fetal, Unspecified
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Brain striatum
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(3)
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(2)
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Epithelial
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Gingival, Gum
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Kidney, Kidney
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Lens, Eye
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Muscle, Unspecified
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Peripheral Vein
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Skin, Chest
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Skin, Flank
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Umbilical Cord, Umbilical cord
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Male
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Other
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More than one race
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Asian
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Other
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Unknown
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East Indian
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(16)
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Caucasian
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Filipino
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Chinese
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Korean
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Japanese
(1)
dbGap Data Available:
No
(23177)
Yes
(3245)
Extended Clinical Data Available:
No
(13405)
Yes
(13017)
Age at Sampling (Years):
55-64
(3461)
65-74
(3115)
45-54
(3058)
35-44
(2899)
25-34
(1979)
75-89
(1959)
15-24
(1576)
5-14
(1492)
0-4
(1052)
90-99
(44)
100+
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