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Search Results for -
ADRENAL HYPOPLASIA WITH ADDITIONAL CONGENITAL MALFORMATIONS
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Also searched for:
ADDISON DISEASE, X-LINKED
ADRENAL HYPOPLASIA, CONGENITAL
ADRENAL HYPOPLASIA, CONGENITAL, WITH HYPOGONADOTROPIC HYPOGONADISM
AHC
AHC WITH HHG
AHC WITH ISOLATED GONADOTROPIN DEFICIENCY
AHCH
AHX
CAH - CONGENITAL ADRENAL HYPOPLASIA
CONGENITAL ADRENAL HYPOPLASIA
CONGENITAL HYPOPLASIA OF ADRENAL GLAND
CONGENITAL SMALL ADRENAL GLAND
CYTOMEGALIC ADRENOCORTICAL HYPOPLASIA
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Repository:
NINDS Repository
(27294)
NIGMS Human Genetic Cell Repository
(18070)
NHGRI Sample Repository for Human Genetic Research
(7468)
NIA Aging Cell Culture Repository
(4132)
Autism
(362)
HD Community Biorepository
(49)
Centers for Disease Control and Prevention Repository
(18)
Human Reference Genetic Material Repository
(1)
Collection:
Heritable Diseases
(11543)
NHGRI Sample Repository for Human Genetic Research
(7468)
Parkinsonism
(6678)
Cerebrovascular Disease
(6453)
Control
(6385)
Motor Neuron Disease
(5129)
Epilepsy
(3433)
Chromosome Abnormalities
(2873)
Human Variation
(1897)
CEPH
(1615)
Apparently Healthy Collection
(1608)
dbGaP
(1324)
PIGI Consented Sample
(1302)
Old Order Amish Major Affective Disorder
(1006)
Repository Linkage Families
(816)
GRC
(782)
Lysosomal Storage Diseases
(747)
University of Georgia Centenarian Study
(716)
Tourette Syndrome
(645)
Hybrids
(556)
Muscular Dystrophies
(553)
GeT-RM Samples
(510)
Animals
(495)
Hereditary Cancers
(391)
Pharmacogenetics
(333)
The 90+ Study
(331)
CMD Specific
(278)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(260)
Alzheimer's Disease
(249)
Venezuelan Huntington Disease
(243)
Canadian Alzheimer Disease
(226)
Disorders of the Urea Cycle
(226)
Dystonia
(225)
Maturity-Onset Diabetes of the Young
(222)
Retinitis Pigmentosa Foundation Collection
(195)
Italian Alzheimer Disease
(120)
Nonhuman Primates
(112)
German Alzheimer Disease
(99)
FOXG1
(93)
Stem Cell Collection
(87)
Aged Sib Pairs
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DGAP
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Whole-Genome Sequence
(51)
Ames Dwarf Mice
(43)
Alzheimer Disease With No Family History
(31)
Non-Healing Wound Collection
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Engineered Cell Cultures
(15)
Apparently healthy iPSCs
(13)
Gene-Edited hiPSC
(11)
Specially Characterized Fibroblasts
(11)
Frontotemporal Degeneration
(4)
Prostate Cancer
(3)
Additional PSP subjects (others grouped with Parkinsonism)
(1)
Product:
LCL
(25944)
DNA
(25774)
Fibroblast
(4826)
Somatic cell hybrid
(320)
iPSC
(129)
mESC
(87)
High Molecular Weight DNA
(71)
Smooth muscle
(61)
Endothelial
(47)
Plasmid
(37)
Preprocessed DNA
(20)
Epithelial
(15)
Tumor-derived cell line
(15)
Neuronally-derived
(10)
Amniotic fluid-derived cell line
(7)
Hybridoma
(7)
Myeloma
(7)
Mesothelial
(4)
Chorionic villus-derived cell line
(2)
Erythroleukemic cell line
(2)
Kidney-derived cell line
(2)
Adipose stromal cell
(1)
Antibodies
(1)
Cytoplasmic transfer (cybrid)
(1)
FFPE
(1)
Microcell hybrid
(1)
Protein
(1)
Affected:
Yes
(26563)
No
(14325)
Unknown
(3162)
At Risk
(2857)
Mutation Data Available:
N
(51451)
Y
(5943)
Source:
B-Lymphocyte
(26009)
LCL
(21570)
Whole Blood
(2528)
Fibroblast
(1532)
Skin, Arm
(1071)
Skin, Unspecified
(483)
Somatic cell hybrid
(236)
Skin, Skin
(231)
Lung, Lung
(106)
Skin, Ear
(65)
Skin, Thigh
(65)
Skin, Foreskin
(59)
Aorta, thoracic
(57)
Skin, Abdomen
(27)
Blood
(21)
Fetal, Unspecified
(12)
Skin, Leg
(12)
Skin, Posterior iliac crest
(12)
Trachealis muscle
(12)
Vein, iliac
(11)
Brain striatum
(10)
Gonad, Gonad
(10)
Skin, Thorax
(10)
Skin, Thorax/abdomen
(10)
Artery, iliac
(9)
Artery, pulmonary
(9)
Skin, Buttock
(9)
Umbilical Cord, Umbilical cord
(9)
Skin, Back
(8)
Skin, Buttock-thigh
(8)
Skin, Inguinal area
(8)
Skin, Sacrum
(8)
Amniotic fluid
(7)
Gonad, Ovary
(7)
Whole embryo, Embryo
(7)
Breast organoid
(6)
Muscle, Unspecified
(6)
Conjunctiva, Conjunctiva
(5)
Epithelial
(5)
Liver, Liver
(5)
Placental, Placenta
(5)
Retina of eye
(5)
Skin, Fetal
(5)
Skin, Hip
(5)
Skin, Right ischium
(5)
Embryonal carcinoma
(4)
Eye
(4)
Gingival, Gum
(4)
Amniotic fluid-derived cell line
(3)
Gonad, Testes
(3)
Kidney, Kidney
(3)
Leiomyoma
(3)
Skin, Genital area
(3)
Skin, Toe
(3)
Smooth muscle
(3)
Amnion, Amnion
(2)
Aorta, abdominal
(2)
Aortic arch
(2)
Ascites fluid
(2)
Bladder carcinoma
(2)
Chorionic villus
(2)
Endometrial, Uterus
(2)
Heart, Pericardium
(2)
Kidney
(2)
Lung
(2)
Mesothelial
(2)
Skin, Calf
(2)
Skin, Chest
(2)
Skin, Labialscrotal fold
(2)
Skin, Neck
(2)
Skin, Shoulder
(2)
Skin, Thoraco-lumbar junction
(2)
Skin, Umbilical area
(2)
Spleen, Keloid
(2)
T-Lymphocyte
(2)
Tendon, Achilles tendon
(2)
Tumor
(2)
Tumor, Fibroma
(2)
Tumor-derived cell line
(2)
Umbilical Cord, Vein, umbilical
(2)
Vein, umbilical
(2)
Adenocarcinoma
(1)
Adrenal cortex tumor
(1)
Artery, Aorta, thoracic
(1)
Artery, carotid
(1)
Ascites fluid, Ascites fluid
(1)
Brain, Brain
(1)
Brain, Unspecified
(1)
Cartilage, Nasal
(1)
Cartilage, Unspecified
(1)
Cervix, Cerivix uteri
(1)
Chest
(1)
Chorionic villus-derived cell line
(1)
Cornea, Cornea
(1)
Endothelial
(1)
Ewing sarcoma
(1)
Fetal, Arm
(1)
Heart, Unspecified
(1)
Lens, Eye
(1)
Ligament, Teeth
(1)
Sex:
Female
(28840)
Male
(27690)
Other
(26)
Race:
White
(37711)
Black/African American
(3386)
Asian
(802)
More than one race
(684)
Other
(586)
Unknown
(442)
Hispanic/Latino
(336)
Caucasian
(316)
Asiatic Indian
(254)
Chinese
(217)
American Indian/Alaska Native
(135)
Native Hawaiian/Other Pacific Islander
(74)
East Indian
(62)
Not Reported
(45)
Asian, Other
(30)
Filipino
(10)
Korean
(6)
Japanese
(3)
Vietnamese
(3)
dbGap Data Available:
No
(49407)
Yes
(7987)
Extended Clinical Data Available:
No
(29279)
Yes
(28115)
Age at Sampling (Years):
45-54
(7214)
55-64
(7139)
35-44
(5866)
65-74
(5587)
25-34
(4563)
5-14
(4170)
15-24
(3687)
0-4
(3546)
75-89
(3287)
90-99
(638)
100+
(227)
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