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Search Results for -
BILATERAL CONGENITAL ABSENCE OF KIDNEYS
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Also searched for:
BRA - BILATERAL RENAL AGENESIS
CONGENITAL ABSENCE OF KIDNEYS SYNDROME
HEREDITARY RENAL APLASIA
HRA
POTTER SYNDROME
POTTER'S ANOMALY OF THE KIDNEY
RENAL ADYSPLASIA
RENAL AGENESIS
RENAL AGENESIS SYNDROME
RENAL APLASIA
RENOFACIAL SYNDROME
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Repository:
NIGMS Human Genetic Cell Repository
(12157)
NHGRI Sample Repository for Human Genetic Research
(6705)
NINDS Repository
(5199)
NIA Aging Cell Culture Repository
(4120)
HD Community Biorepository
(190)
Autism
(24)
Centers for Disease Control and Prevention Repository
(24)
Orphan Disease Center
(8)
Allen Cell Collection
(4)
Collection:
Heritable Diseases
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NHGRI Sample Repository for Human Genetic Research
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Cerebrovascular Disease
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Control
(1689)
Chromosome Abnormalities
(1595)
Human Variation
(1362)
Apparently Healthy Collection
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Old Order Amish Major Affective Disorder
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University of Georgia Centenarian Study
(855)
PIGI Consented Sample
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Motor Neuron Disease
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dbGaP
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GRC
(784)
Parkinsonism
(745)
Lysosomal Storage Diseases
(638)
Hybrids
(552)
Muscular Dystrophies
(521)
GeT-RM Samples
(484)
Hereditary Cancers
(380)
The 90+ Study
(331)
Epilepsy
(324)
Animals
(321)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(260)
CMD Specific
(252)
Venezuelan Huntington Disease
(251)
Alzheimer's Disease
(246)
Pharmacogenetics
(227)
Canadian Alzheimer Disease
(225)
Disorders of the Urea Cycle
(225)
Maturity-Onset Diabetes of the Young
(222)
CEPH
(174)
Retinitis Pigmentosa Foundation Collection
(147)
Italian Alzheimer Disease
(121)
German Alzheimer Disease
(101)
FOXG1
(93)
Repository Linkage Families
(89)
Aged Sib Pairs
(73)
Nonhuman Primates
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Ames Dwarf Mice
(47)
DGAP
(33)
Alzheimer Disease With No Family History
(30)
Dystonia
(22)
Non-Healing Wound Collection
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Apparently healthy iPSCs
(15)
Whole-Genome Sequence
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Engineered Cell Cultures
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Gene-Edited hiPSC
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Tourette Syndrome
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Specially Characterized Fibroblasts
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Prostate Cancer
(3)
Frontotemporal Degeneration
(2)
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DNA
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LCL
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Somatic cell hybrid
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iPSC
(139)
96 well plate of DNA samples
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Smooth muscle
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human variation panel
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High Molecular Weight DNA
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Endothelial
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Adipose stromal cell
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Amniotic fluid-derived cell line
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Epithelial
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Tumor-derived cell line
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Antibodies
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Neuronally-derived
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Chorionic villus-derived cell line
(4)
Mesothelial
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aging mapping panel
(4)
Hybridoma
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Antigen
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Cytoplasmic transfer (cybrid)
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FFPE
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Keratinocyte
(1)
Kidney-derived cell line
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Microcell hybrid
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Myeloma
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gene mutation panel
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Affected:
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(9419)
No
(8390)
Unknown
(2940)
At Risk
(585)
Mutation Data Available:
N
(23450)
Y
(4866)
No
(115)
Source:
B-Lymphocyte
(11591)
LCL
(8526)
Whole Blood
(2499)
Fibroblast
(1142)
Skin, Arm
(1036)
Skin, Unspecified
(414)
Somatic cell hybrid
(233)
Skin, Skin
(193)
Lung, Lung
(94)
Skin, Ear
(64)
Aorta, thoracic
(54)
Skin, Thigh
(49)
Skin, Abdomen
(30)
Skin, Foreskin
(18)
Amniotic fluid
(17)
Brain striatum
(12)
Trachealis muscle
(12)
Vein, iliac
(11)
Skin, Buttock
(10)
Skin, Thorax
(10)
Skin, Thorax/abdomen
(10)
Amniotic fluid-derived cell line
(9)
Artery, pulmonary
(9)
Artery, iliac
(8)
Skin, Buttock-thigh
(8)
Skin, Leg
(8)
Skin, Sacrum
(8)
Whole embryo, Embryo
(8)
Blood
(7)
Skin, Posterior iliac crest
(7)
Stem cell
(7)
Umbilical Cord, Umbilical cord
(7)
Breast organoid
(6)
Skin, Back
(6)
Conjunctiva, Conjunctiva
(5)
Epithelial
(5)
Retina of eye
(5)
Skin, Hip
(5)
Skin, Right ischium
(5)
Chorionic villus
(4)
Embryonal carcinoma
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Eye
(4)
Fetal, Unspecified
(4)
Gonad, Ovary
(4)
Liver, Liver
(4)
Chorionic villus-derived cell line
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Gingival, Gum
(3)
Gonad, Gonad
(3)
Gonad, Testes
(3)
Muscle, Unspecified
(3)
Placental, Placenta
(3)
Skin, Fetal
(3)
Skin, Inguinal area
(3)
Skin, Toe
(3)
Smooth muscle
(3)
Aortic arch
(2)
Ascites fluid
(2)
Bladder carcinoma
(2)
Endometrial, Uterus
(2)
Kidney, Kidney
(2)
Leiomyoma
(2)
Lung
(2)
Mesothelial
(2)
Skin, Neck
(2)
T-Lymphocyte
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Tumor
(2)
Tumor-derived cell line
(2)
Umbilical Cord, Vein, umbilical
(2)
Adenocarcinoma
(1)
Adrenal cortex tumor
(1)
Amnion, Amnion
(1)
Aorta, abdominal
(1)
Artery, Aorta, thoracic
(1)
Artery, carotid
(1)
Ascites fluid, Ascites fluid
(1)
Brain, Unspecified
(1)
Cartilage, Nasal
(1)
Cartilage, Unspecified
(1)
Cervix, Cerivix uteri
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Chest
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Endothelial
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Ewing sarcoma
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Fetal, Arm
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Heart, Pericardium
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Heart, Unspecified
(1)
Kidney
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Lens, Eye
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Ligament, Teeth
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Neuroepithelioma
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Osteosarcoma
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Peripheral Vein
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Polyp, Nasal
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Skin, Axilla
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Skin, Calf
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Skin, Chest
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Skin, Flank
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Skin, Foot
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Skin, Genital area
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Skin, Labialscrotal fold
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Skin, Omentum
(1)
Sex:
Female
(14542)
Male
(12904)
Other
(9)
Race:
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(15169)
Black/African American
(1114)
Hispanic/Latino
(309)
Asian
(293)
Chinese
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Other
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More than one race
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Unknown
(80)
East Indian
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Not Reported
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Asiatic Indian
(36)
American Indian/Alaska Native
(27)
Caucasian
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Asian, Other
(24)
Native Hawaiian/Other Pacific Islander
(20)
Filipino
(10)
Korean
(5)
Japanese
(3)
Vietnamese
(3)
dbGap Data Available:
No
(26940)
Yes
(1491)
Extended Clinical Data Available:
No
(22741)
Yes
(5690)
Age at Sampling (Years):
35-44
(2685)
45-54
(2630)
25-34
(2522)
15-24
(2261)
55-64
(2182)
5-14
(2032)
0-4
(1965)
65-74
(1511)
75-89
(938)
90-99
(582)
100+
(233)
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