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Search Results for -
KALLMANN SYNDROME 2
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Also searched for:
HH2
HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM, ANOSMIA- 147950, 244200, 308700
KAL2
KALLMANN SYN
30386 results -
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Repository:
NINDS Repository
(12865)
NIGMS Human Genetic Cell Repository
(12151)
NHGRI Sample Repository for Human Genetic Research
(2682)
NIA Aging Cell Culture Repository
(2565)
Autism
(88)
Orphan Disease Center
(13)
Centers for Disease Control and Prevention Repository
(12)
Allen Cell Collection
(7)
HD Community Biorepository
(3)
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Heritable Diseases
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Tourette Syndrome
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Epilepsy
(2815)
NHGRI Sample Repository for Human Genetic Research
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Parkinsonism
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Chromosome Abnormalities
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Control
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Motor Neuron Disease
(1422)
Human Variation
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Cerebrovascular Disease
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Old Order Amish Major Affective Disorder
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PIGI Consented Sample
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dbGaP
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Animals
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Repository Linkage Families
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Hybrids
(233)
CMD Specific
(197)
Canadian Alzheimer Disease
(185)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(156)
Pharmacogenetics
(149)
Alzheimer's Disease
(148)
University of Georgia Centenarian Study
(144)
Venezuelan Huntington Disease
(127)
Disorders of the Urea Cycle
(119)
Dystonia
(114)
Italian Alzheimer Disease
(108)
FOXG1
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German Alzheimer Disease
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Nonhuman Primates
(66)
Retinitis Pigmentosa Foundation Collection
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Maturity-Onset Diabetes of the Young
(58)
The 90+ Study
(51)
Aged Sib Pairs
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DGAP
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Ames Dwarf Mice
(44)
Stem Cell Collection
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Whole-Genome Sequence
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Alzheimer Disease With No Family History
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Gene-Edited hiPSC
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Non-Healing Wound Collection
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Apparently healthy iPSCs
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Engineered Cell Cultures
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Frontotemporal Degeneration
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Human Pangenome Reference Collection
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Prostate Cancer
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Specially Characterized Fibroblasts
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DNA
(15965)
LCL
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(3814)
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(145)
iPSC
(145)
High Molecular Weight DNA
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mESC
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human variation panel
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Chorionic villus-derived cell line
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Mesothelial
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Neuronally-derived
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hybrid mapping panel
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Erythroleukemic cell line
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FFPE
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aging mapping panel
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gene mutation panel
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hybrid regional mapping panel
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Affected:
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(13921)
No
(7579)
At Risk
(3208)
Unknown
(1356)
Mutation Data Available:
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(25378)
Y
(4997)
No
(11)
Source:
B-Lymphocyte
(10122)
LCL
(7477)
Whole Blood
(7336)
Fibroblast
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Skin, Arm
(986)
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Skin, Skin
(214)
Somatic cell hybrid
(88)
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(53)
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(51)
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(50)
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(39)
Amniotic fluid
(30)
Blood
(24)
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(24)
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(23)
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(12)
Amniotic fluid-derived cell line
(11)
Skin, Thorax
(10)
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(7)
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Stem cell
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(5)
Liver, Liver
(5)
Placental, Placenta
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Skin, Buttock-thigh
(5)
Skin, Hip
(5)
Skin, Inguinal area
(5)
Skin, Sacrum
(5)
Umbilical Cord, Umbilical cord
(5)
Vein, iliac
(5)
Fetal, Unspecified
(4)
Gonad, Gonad
(4)
Muscle, Unspecified
(4)
Artery, pulmonary
(3)
Breast organoid
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(3)
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(3)
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(3)
Tumor-derived cell line
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Aorta, abdominal
(2)
Brain striatum
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Conjunctiva, Conjunctiva
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Gonad, Testes
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Heart, Pericardium
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Leiomyoma
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Amnion, Amnion
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Aortic arch
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Artery, Aorta, thoracic
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Ascites fluid
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Brain, Unspecified
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Chorionic villus-derived cell line
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Endothelial
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Heart, Unspecified
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Hydatidiform mole
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Lung
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Skin, Shoulder
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Skin, Umbilical area
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(1)
Tumor, Abdomen
(1)
Sex:
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(15650)
Male
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Other
(15)
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(21317)
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(1099)
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Not Reported
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Filipino
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Korean
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Japanese
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dbGap Data Available:
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(25141)
Yes
(5245)
Extended Clinical Data Available:
No
(16979)
Yes
(13407)
Age at Sampling (Years):
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(3734)
35-44
(3606)
45-54
(3251)
15-24
(3037)
25-34
(3008)
55-64
(2899)
0-4
(2307)
65-74
(2296)
75-89
(1344)
90-99
(178)
100+
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