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Search Results for -
MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)
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(and perform an exact match search)
Also searched for:
ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS
ALPERS' DISEASE
ALPER'S DISEASE
ALPERS PROGRESSIVE INFANTILE POLIODYSTROPHY
ALPERS SYNDROME
ALPERS-HUTTENLOCHER SYNDROME
GRAY MATTER DEGENERATION
MTDPS4A
NEURONAL DEGENERATION OF CHILDHOOD WITH LIVER DISEASE, PROGRESSIVE
PNDC
POLIODYSTROPHY
PROGRESSIVE NEURONAL DEGENERATION WITH LIVER CIRRHOSIS
PROGRESSIVE SCLEROSING POLIODYSTROPHY
SPONGY GLIONEURONAL DYSTROPHY
63906 results -
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Repository:
NINDS Repository
(43725)
NIGMS Human Genetic Cell Repository
(11417)
NHGRI Sample Repository for Human Genetic Research
(3753)
AREDS
(2931)
NIA Aging Cell Culture Repository
(1689)
Autism
(184)
HD Community Biorepository
(164)
Centers for Disease Control and Prevention Repository
(27)
Orphan Disease Center
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Allen Cell Collection
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CIMR Research
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Human Reference Genetic Material Repository
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Cerebrovascular Disease
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Control
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Parkinsonism
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Epilepsy
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Motor Neuron Disease
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Tourette Syndrome
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Dystonia
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NHGRI Sample Repository for Human Genetic Research
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Chromosome Abnormalities
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Human Variation
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CEPH
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PIGI Consented Sample
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Apparently Healthy Collection
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Old Order Amish Major Affective Disorder
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dbGaP
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University of Georgia Centenarian Study
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Michigan
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GeT-RM Samples
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Massachusetts
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Illinois
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Pennsylvania
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Canadian Alzheimer Disease
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Maturity-Onset Diabetes of the Young
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GRC
(140)
"Intra-abdominal fat and risk of disease in children and adolescents" study
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CMD Specific
(123)
Disorders of the Urea Cycle
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Alzheimer's Disease
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FOXG1
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Retinitis Pigmentosa Foundation Collection
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Animals
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German Alzheimer Disease
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Italian Alzheimer Disease
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Oregon
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DGAP
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Whole-Genome Sequence
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Wisconsin
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Apparently healthy iPSCs
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New York
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Johns Hopkins University
(2)
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Nonhuman Primates
(1)
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DNA
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LCL
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Fibroblast
(2084)
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(164)
iPSC
(115)
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(85)
96 well plate of DNA samples
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High Molecular Weight DNA
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Preprocessed DNA
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aging mapping panel
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hybrid mapping panel
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Keratinocyte
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Microcell hybrid
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gene mutation panel
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Affected:
Yes
(37165)
No
(11826)
At Risk
(5060)
Unknown
(1586)
Mutation Data Available:
N
(59392)
Y
(4436)
No
(78)
Source:
Whole Blood
(30662)
LCL
(22601)
B-Lymphocyte
(6360)
Fibroblast
(1490)
Skin, Unspecified
(304)
Somatic cell hybrid
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(225)
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(167)
Skin, Thigh
(41)
Lung, Lung
(34)
Amniotic fluid-derived cell line
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Blood
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Amniotic fluid
(15)
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(9)
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Stem cell
(7)
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(6)
Epithelial
(5)
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(4)
Umbilical Cord, Umbilical cord
(4)
Chorionic villus-derived cell line
(3)
Conjunctiva, Conjunctiva
(3)
Fetal, Unspecified
(3)
Gonad, Gonad
(3)
Kidney, Kidney
(3)
Liver, Liver
(3)
Muscle, Unspecified
(3)
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(3)
Skin, Hip
(3)
Skin, Thorax/abdomen
(3)
Smooth muscle
(3)
Tumor-derived cell line
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Mesothelial
(2)
Placental, Placenta
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(2)
Skin, Fetal
(2)
Skin, Foreskin
(2)
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(2)
T-Lymphocyte
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Amnion, Amnion
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Cartilage, Nasal
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Cartilage, Unspecified
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Chest
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Chorionic villus
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Cornea, Cornea
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Endothelial
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Ewing sarcoma
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Gonad, Testes
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Heart, Pericardium
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Heart, Unspecified
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Ligament, Teeth
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Skin, Axilla
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Tumor
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(1)
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(1)
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(1)
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(1)
Umbilical Cord, Vein, umbilical
(1)
Sex:
Female
(32101)
Male
(30007)
Other
(15)
Race:
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Black/African American
(6035)
More than one race
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Asian
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Other
(884)
Unknown
(605)
American Indian/Alaska Native
(249)
Hispanic/Latino
(235)
Caucasian
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Chinese
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Native Hawaiian/Other Pacific Islander
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Not Reported
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Asian, Other
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Filipino
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Korean
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Japanese
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Vietnamese
(2)
dbGap Data Available:
No
(52434)
Yes
(11472)
Extended Clinical Data Available:
Yes
(44139)
No
(19767)
Age at Sampling (Years):
55-64
(9513)
45-54
(8505)
65-74
(7956)
35-44
(6778)
25-34
(4865)
5-14
(4560)
75-89
(4445)
15-24
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0-4
(2123)
90-99
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100+
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