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Samples (27172)
Website Content (540)

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DNA (11756)
LCL (10750)
Fibroblast (3596)
Somatic cell hybrid (317)
iPSC (173)
Plasmid (165)
High Molecular Weight DNA (70)
96 well plate of DNA samples (62)
Smooth muscle (60)
human variation panel (49)
Endothelial (41)
Adipose stromal cell (23)
Amniotic fluid-derived cell line (17)
Antibodies (17)
Epithelial (15)
Tumor-derived cell line (15)
Neuronally-derived (12)
Collection of iPSC (8)
Chorionic villus-derived cell line (4)
Mesothelial (4)
aging mapping panel (4)
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Protein (2)
Antigen (1)
Cytoplasmic transfer (cybrid) (1)
FFPE (1)
Keratinocyte (1)
Kidney-derived cell line (1)
Microcell hybrid (1)
Myeloma (1)
Peptide (1)
gene mutation panel (1)

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B-Lymphocyte (10817)
LCL (7819)
Whole Blood (2610)
Fibroblast (1209)
Skin, Arm (1034)
Skin, Unspecified (414)
Somatic cell hybrid (232)
Skin, Skin (204)
Lung, Lung (89)
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Aorta, thoracic (54)
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Skin, Abdomen (30)
Blood (25)
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Amniotic fluid (17)
Stem cell (14)
Brain striatum (12)
Trachealis muscle (12)
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Vein, iliac (11)
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)
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Umbilical Cord, Umbilical cord (7)
Breast organoid (6)
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Conjunctiva, Conjunctiva (5)
Epithelial (5)
Retina of eye (5)
Skin, Hip (5)
Skin, Right ischium (5)
Chorionic villus (4)
Embryonal carcinoma (4)
Eye (4)
Fetal, Unspecified (4)
Gonad, Ovary (4)
Liver, Liver (4)
Chorionic villus-derived cell line (3)
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 (2)
Tumor (2)
Tumor-derived cell line (2)
Umbilical Cord, Vein, umbilical (2)
Adenocarcinoma (1)
Adrenal cortex tumor (1)
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Aorta, abdominal (1)
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Artery, carotid (1)
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Skin, Genital area (1)
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NIGMS Human Genetic Cell Repository (12393)
NINDS Repository (5319)
NHGRI Sample Repository for Human Genetic Research (4998)
NIA Aging Cell Culture Repository (4153)
HD Community Biorepository (196)
NIAID - USIDnet (41)
Autism (24)
Centers for Disease Control and Prevention Repository (24)
Allen Cell Collection (14)
Orphan Disease Center (10)

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Other (9)

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White (15465)
Black/African American (1127)
Hispanic/Latino (310)
Asian (308)
Chinese (218)
Other (216)
More than one race (208)
Unknown (87)
East Indian (57)
Not Reported (46)
Asiatic Indian (37)
American Indian/Alaska Native (29)
Caucasian (29)
Asian, Other (25)
Native Hawaiian/Other Pacific Islander (20)
Filipino (10)
Korean (5)
Japanese (3)
Vietnamese (3)

Affected:

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Yes (9723)
No (8493)
Unknown (2612)
At Risk (590)

Mutation Data Available:

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N (22049)
Y (5003)
No (120)

Age at Sampling (Years):

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0-4 (2001)
5-14 (2098)
15-24 (2304)
25-34 (2586)
35-44 (2745)
45-54 (2678)
55-64 (2220)
65-74 (1557)
75-89 (949)
90-99 (583)
100+ (237)

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Heritable Diseases (9334)
NHGRI Sample Repository for Human Genetic Research (4998)
Cerebrovascular Disease (2808)
Control (1691)
Chromosome Abnormalities (1613)
Human Variation (1373)
Apparently Healthy Collection (1070)
Old Order Amish Major Affective Disorder (966)
PIGI Consented Sample (922)
University of Georgia Centenarian Study (859)
GRC (815)
Motor Neuron Disease (810)
dbGaP (804)
Parkinsonism (746)
Lysosomal Storage Diseases (673)
Muscular Dystrophies (575)
Hybrids (549)
GeT-RM Samples (489)
Hereditary Cancers (384)
The 90+ Study (331)
Epilepsy (326)
Animals (321)
CMD Specific (276)
"Intra-abdominal fat and risk of disease in children and adolescents" study (260)
Venezuelan Huntington Disease (251)
Alzheimer's Disease (247)
Disorders of the Urea Cycle (230)
Pharmacogenetics (227)
Canadian Alzheimer Disease (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 (58)
Ames Dwarf Mice (47)
DGAP (34)
Alzheimer Disease With No Family History (29)
Dystonia (22)
Apparently healthy iPSCs (18)
Non-Healing Wound Collection (17)
Whole-Genome Sequence (15)
Engineered Cell Cultures (14)
Gene-Edited hiPSC (14)
Tourette Syndrome (12)
Specially Characterized Fibroblasts (11)
Cardiomyopathy (6)
Prostate Cancer (3)
Frontotemporal Degeneration (2)
Laminopathy (1)
Skeletal Myopathy (1)

dbGap Data Available:

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Yes (1475)

Extended Clinical Data Available:

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No (21307)
Yes (5865)

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Search Results for - BILATERAL CONGENITAL ABSENCE OF KIDNEYS

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Catalog Items
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Description
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Description

Product

Source

(Showing Items: 50)

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GM23377

RENAL ADYSPLASIA

Fibroblast

Skin, Unspecified

View

GM11071

RENAL ADYSPLASIA

Fibroblast

View

GM21261

ROKITANSKY-KUSTER-HAUSER SYNDROME | RENAL ADYSPLASIA

LCL

B-Lymphocyte

View

NA21261

ROKITANSKY-KUSTER-HAUSER SYNDROME | RENAL ADYSPLASIA

DNA

LCL

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NA13242

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

DNA

LCL

View

GM13242

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

LCL

B-Lymphocyte

View

GM21496

ROKITANSKY-KUSTER-HAUSER SYNDROME

LCL

B-Lymphocyte

View

NA21496

ROKITANSKY-KUSTER-HAUSER SYNDROME

DNA

LCL

View

NA13276

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

DNA

LCL

View

GM13276

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

LCL

B-Lymphocyte

View

GM09562

CHROMOSOME DELETION

LCL

B-Lymphocyte

View

NA26595

CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1

DNA

LCL

View

GM26595

CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1

LCL

B-Lymphocyte

View

GM26596

CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1

Fibroblast

Skin, Arm

View

GM13298

ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM

Fibroblast

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GM12895

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR

LCL

B-Lymphocyte

View

NA12895

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR

DNA

LCL

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GM24265

TRANSLOCATED CHROMOSOME

LCL

B-Lymphocyte

View

NA08299

TUBEROUS SCLEROSIS 2; TSC2 | TSC2 GENE; TSC2

DNA

LCL

View

GM08299

TUBEROUS SCLEROSIS 2; TSC2 | TSC2 GENE; TSC2

LCL

B-Lymphocyte

View

GM13343

LIPASE, CONGENITAL ABSENCE OF PANCREATIC

LCL

B-Lymphocyte

View

GM13322

LIPASE, CONGENITAL ABSENCE OF PANCREATIC

LCL

B-Lymphocyte

View

GM13344

LIPASE, CONGENITAL ABSENCE OF PANCREATIC

LCL

B-Lymphocyte

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GM13278

LIPASE, CONGENITAL ABSENCE OF PANCREATIC

LCL

B-Lymphocyte

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GM26607

CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1

Fibroblast

Skin, Arm

View

GM12690

ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY; EAD

LCL

B-Lymphocyte

View

GM20949

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic | ALG6, S. CEREVISIAE, HOMOLOG OF

Fibroblast

Skin, Unspecified

View

NA20949

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic | ALG6, S. CEREVISIAE, HOMOLOG OF

DNA

Fibroblast

View

GM08296

TUBEROUS SCLEROSIS 2; TSC2 | TSC2 GENE; TSC2

LCL

B-Lymphocyte

View

NA08296

TUBEROUS SCLEROSIS 2; TSC2 | TSC2 GENE; TSC2

DNA

LCL

View

GM16002

NODAL RHYTHM

LCL

B-Lymphocyte

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GM16008

NODAL RHYTHM

LCL

B-Lymphocyte

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GM16019

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16007

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16005

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16006

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16011

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16009

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16004

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16020

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM16010

NODAL RHYTHM

LCL

B-Lymphocyte

View

GM03577

DIGEORGE SYNDROME; DGS | TRANSLOCATED CHROMOSOME

Fibroblast

View

NA03577

DIGEORGE SYNDROME; DGS | TRANSLOCATED CHROMOSOME

DNA

Fibroblast

View

GM11592

VERTEBRAL ANOMALIES

LCL

B-Lymphocyte

View

NA12590

TRANSLOCATED CHROMOSOME

DNA

Amniotic fluid-derived cell line

View

GM12590

TRANSLOCATED CHROMOSOME

Amniotic fluid-derived cell line

Amniotic fluid

View

GM09706

RING CHROMOSOME

LCL

B-Lymphocyte

View

NA09706

RING CHROMOSOME

DNA

LCL

View

GM23670

MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A

LCL

B-Lymphocyte

View

GM26244

MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2

LCL

B-Lymphocyte

No Results were Found

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