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Samples (38214)
Website Content (1593)

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DNA (20271)
LCL (13047)
Fibroblast (3744)
Somatic cell hybrid (318)
iPSC (257)
Plasmid (165)
96 well plate of DNA samples (62)
Smooth muscle (60)
High Molecular Weight DNA (57)
human variation panel (49)
Endothelial (44)
Adipose stromal cell (23)
Amniotic fluid-derived cell line (20)
Antibodies (17)
Epithelial (15)
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Neuronally-derived (12)
Collection of iPSC (8)
Protein (5)
Chorionic villus-derived cell line (4)
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aging mapping panel (4)
Hybridoma (2)
Kidney-derived cell line (2)
Antigen (1)
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FFPE (1)
Keratinocyte (1)
Microcell hybrid (1)
Myeloma (1)
Peptide (1)
gene mutation panel (1)

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B-Lymphocyte (13106)
LCL (9891)
Whole Blood (9066)
Fibroblast (1235)
Skin, Arm (1040)
Skin, Unspecified (418)
Somatic cell hybrid (234)
Skin, Skin (201)
Lung, Lung (94)
Skin, Ear (64)
Blood (63)
Skin, Thigh (55)
Aorta, thoracic (54)
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Amniotic fluid (20)
Skin, Foreskin (18)
Brain striatum (12)
Stem cell (12)
Trachealis muscle (12)
Vein, iliac (11)
Skin, Buttock (10)
Skin, Thorax (10)
Skin, Thorax/abdomen (10)
Artery, iliac (9)
Artery, pulmonary (9)
Amniotic fluid-derived cell line (8)
Skin, Buttock-thigh (8)
Skin, Leg (8)
Skin, Sacrum (8)
Whole embryo, Embryo (8)
Skin, Back (7)
Skin, Posterior iliac crest (7)
Breast organoid (6)
Skin, Hip (6)
Umbilical Cord, Umbilical cord (6)
Conjunctiva, Conjunctiva (5)
Epithelial (5)
Fetal, Unspecified (5)
Retina of eye (5)
Skin, Right ischium (5)
Chorionic villus (4)
Embryonal carcinoma (4)
Eye (4)
Gonad, Ovary (4)
Liver, Liver (4)
Skin, Fetal (4)
Chorionic villus-derived cell line (3)
Gingival, Gum (3)
Gonad, Gonad (3)
Gonad, Testes (3)
Kidney, Kidney (3)
Muscle, Unspecified (3)
Placental, Placenta (3)
Skin, Inguinal area (3)
Skin, Toe (3)
Smooth muscle (3)
Aorta, abdominal (2)
Aortic arch (2)
Ascites fluid (2)
Bladder carcinoma (2)
Endometrial, Uterus (2)
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Kidney (2)
Leiomyoma (2)
Lung (2)
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Skin, Thoraco-lumbar junction (2)
Spleen, Keloid (2)
T-Lymphocyte (2)
Tumor (2)
Tumor-derived cell line (2)
Vein, umbilical (2)
Adenocarcinoma (1)
Adrenal cortex tumor (1)
Amnion, Amnion (1)
Artery, Aorta, thoracic (1)
Artery, carotid (1)
Ascites fluid, Ascites fluid (1)
Brain, Brain (1)
Brain, Unspecified (1)
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Ewing sarcoma (1)
Fetal, Arm (1)
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Lens, Eye (1)
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Osteosarcoma (1)
Peripheral Vein (1)
Polyp, Nasal (1)
Skin, Axilla (1)
Skin, Calf (1)
Skin, Chest (1)
Skin, Flank (1)
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NINDS Repository (15207)
NIGMS Human Genetic Cell Repository (12771)
NHGRI Sample Repository for Human Genetic Research (5727)
NIA Aging Cell Culture Repository (4194)
HD Community Biorepository (199)
NIAID - USIDnet (43)
Autism (24)
Centers for Disease Control and Prevention Repository (24)
Allen Cell Collection (14)
Orphan Disease Center (10)
Human Reference Genetic Material Repository (1)

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Other (7)

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White (21398)
Black/African American (3767)
More than one race (1068)
Unknown (506)
Asian (468)
Hispanic/Latino (346)
Other (300)
Chinese (216)
American Indian/Alaska Native (59)
Not Reported (56)
East Indian (55)
Asiatic Indian (33)
Asian, Other (31)
Caucasian (30)
Native Hawaiian/Other Pacific Islander (22)
Filipino (10)
Korean (5)
Japanese (3)
Vietnamese (2)

Affected:

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Yes (16805)
No (10178)
Unknown (2914)
At Risk (2067)

Mutation Data Available:

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N (32206)
Y (5887)
No (121)

Age at Sampling (Years):

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0-4 (2557)
5-14 (3393)
15-24 (3181)
25-34 (3469)
35-44 (3829)
45-54 (3816)
55-64 (4029)
65-74 (3250)
75-89 (1827)
90-99 (603)
100+ (237)

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Heritable Diseases (9596)
NHGRI Sample Repository for Human Genetic Research (5727)
Epilepsy (5658)
Cerebrovascular Disease (4074)
Control (3238)
Parkinsonism (1913)
Chromosome Abnormalities (1578)
Motor Neuron Disease (1391)
Human Variation (1380)
Apparently Healthy Collection (1244)
PIGI Consented Sample (1092)
Old Order Amish Major Affective Disorder (966)
University of Georgia Centenarian Study (859)
GRC (825)
dbGaP (786)
Lysosomal Storage Diseases (748)
Hybrids (552)
Muscular Dystrophies (552)
GeT-RM Samples (492)
Hereditary Cancers (384)
Animals (336)
The 90+ Study (331)
"Intra-abdominal fat and risk of disease in children and adolescents" study (260)
CMD Specific (254)
Venezuelan Huntington Disease (251)
Alzheimer's Disease (249)
Pharmacogenetics (248)
Disorders of the Urea Cycle (230)
Canadian Alzheimer Disease (227)
Maturity-Onset Diabetes of the Young (222)
Retinitis Pigmentosa Foundation Collection (189)
CEPH (187)
Italian Alzheimer Disease (122)
German Alzheimer Disease (101)
Repository Linkage Families (89)
FOXG1 (88)
Aged Sib Pairs (73)
Nonhuman Primates (67)
Whole-Genome Sequence (60)
Apparently healthy iPSCs (53)
Ames Dwarf Mice (47)
DGAP (39)
Dystonia (33)
Alzheimer Disease With No Family History (30)
Gene-Edited hiPSC (17)
Non-Healing Wound Collection (17)
Engineered Cell Cultures (15)
Tourette Syndrome (13)
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 (4277)

Extended Clinical Data Available:

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Yes (15800)

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Search Results for - POTTER'S ANOMALY OF THE KIDNEY

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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

NA21261

ROKITANSKY-KUSTER-HAUSER SYNDROME | RENAL ADYSPLASIA

DNA

LCL

View

GM21261

ROKITANSKY-KUSTER-HAUSER SYNDROME | RENAL ADYSPLASIA

LCL

B-Lymphocyte

View

NA21496

ROKITANSKY-KUSTER-HAUSER SYNDROME

DNA

LCL

View

GM21496

ROKITANSKY-KUSTER-HAUSER SYNDROME

LCL

B-Lymphocyte

View

NA13242

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

DNA

LCL

View

GM13242

VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

LCL

B-Lymphocyte

View

GM26596

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

Fibroblast

Skin, Arm

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

GM24265

TRANSLOCATED CHROMOSOME

LCL

B-Lymphocyte

View

GM25375

SMITH-MAGENIS SYNDROME; SMS

LCL

B-Lymphocyte

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GM10392

FAMILIAL MULTIPLE CONGENITAL ANOMALIES - UNKNOWN SYNDROME OR INHERITANCE

Fibroblast

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GM07071

FRAGILE X MENTAL RETARDATION SYNDROME | FMR1 GENE; FMR1

Fibroblast

Kidney, Kidney

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GM09033

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

Fibroblast

View

GM09032

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

Fibroblast

View

GM05267

MUS

Kidney-derived cell line

Kidney

View

GM12590

TRANSLOCATED CHROMOSOME

Amniotic fluid-derived cell line

Amniotic fluid

View

NA12590

TRANSLOCATED CHROMOSOME

DNA

Amniotic fluid-derived cell line

View

GM12609

POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1

Fibroblast

Kidney, Kidney

View

GM09442

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

Fibroblast

Fetal, Unspecified

View

GM08690

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

Fibroblast

View

GM08740

POLYCYSTIC KIDNEYS

LCL

B-Lymphocyte

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GM10287

POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1

Fibroblast

View

NA06222

CHROMOSOME DELETION

DNA

Fibroblast

View

GM06222

CHROMOSOME DELETION

Fibroblast

View

GM08800

POLYCYSTIC KIDNEYS

LCL

B-Lymphocyte

View

GM08799

POLYCYSTIC KIDNEYS

LCL

B-Lymphocyte

View

GM24143

PERSONAL GENOME PROJECT

LCL

B-Lymphocyte

View

NA24143

PERSONAL GENOME PROJECT

DNA

LCL

View

HM24143

PERSONAL GENOME PROJECT

High Molecular Weight DNA

B-Lymphocyte

View

GM01571

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

Fibroblast

Skin, Unspecified

View

GM03459

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

Fibroblast

View

GM12607

POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1

Fibroblast

Skin, Unspecified

View

GM08372

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

LCL

B-Lymphocyte

View

GM26077

PERSONAL GENOME PROJECT

iPSC

B-Lymphocyte

View

NA13325

DIGEORGE SYNDROME; DGS

DNA

Fibroblast

View

GM07215

DIGEORGE SYNDROME; DGS

Fibroblast

View

GM13325

DIGEORGE SYNDROME; DGS

Fibroblast

View

NA07215

DIGEORGE SYNDROME; DGS

DNA

Fibroblast

View

GM08801

POLYCYSTIC KIDNEYS

LCL

B-Lymphocyte

View

GM04235

HYPOPHOSPHATASIA, INFANTILE | ALKALINE PHOSPHATASE, LIVER; ALPL

Fibroblast

View

GM03859

HYPOPHOSPHATASIA, INFANTILE | ALKALINE PHOSPHATASE, LIVER; ALPL

Fibroblast

View

AG16905

NIA AGING CELL REPOSITORY'S LONGEVITY RESEARCH PROGRAM

LCL

B-Lymphocyte

View

AG16990

NIA AGING CELL REPOSITORY'S LONGEVITY RESEARCH PROGRAM

LCL

B-Lymphocyte

View

GM08698

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

LCL

B-Lymphocyte

View

GM08697

HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510

LCL

B-Lymphocyte

View

GM24147

PERSONAL GENOME PROJECT

LCL

B-Lymphocyte

View

NA03577

DIGEORGE SYNDROME; DGS | TRANSLOCATED CHROMOSOME

DNA

Fibroblast

No Results were Found

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