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Search Results for -
MYASTHENIA GRAVIS, FAMILIAL INFANTILE, 2, FORMERLY
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Also searched for:
CMS IA2
CMS1A2
CMS-EA
CONGENITAL MYASTHENIC SYNDROME TYPE IA2
FAMILIAL INFANTILE MYASTHENIA
FIM
FIM - FAMILIAL INFANTILE MYASTHENIA
FIMG2, FORMERLY
MYASTHENIA, FAMILIAL INFANTILE
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
MYASTHENIC SYNDROME, PRESYNAPTIC, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
27842 results -
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NIGMS Human Genetic Cell Repository
(11156)
NINDS Repository
(10995)
NHGRI Sample Repository for Human Genetic Research
(2682)
NIA Aging Cell Culture Repository
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Autism
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Orphan Disease Center
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Allen Cell Collection
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HD Community Biorepository
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NHGRI Sample Repository for Human Genetic Research
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Repository Linkage Families
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Alzheimer's Disease
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Canadian Alzheimer Disease
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CMD Specific
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Hybrids
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"Intra-abdominal fat and risk of disease in children and adolescents" study
(156)
Pharmacogenetics
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University of Georgia Centenarian Study
(144)
Venezuelan Huntington Disease
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Italian Alzheimer Disease
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Disorders of the Urea Cycle
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German Alzheimer Disease
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Retinitis Pigmentosa Foundation Collection
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Maturity-Onset Diabetes of the Young
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Ames Dwarf Mice
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Alzheimer Disease With No Family History
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Whole-Genome Sequence
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human variation panel
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aging mapping panel
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hybrid mapping panel
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FFPE
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No
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(10023)
LCL
(7607)
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Skin, Inguinal area
(5)
Skin, Sacrum
(5)
Umbilical Cord, Umbilical cord
(5)
Vein, iliac
(5)
Fetal, Unspecified
(4)
Muscle, Unspecified
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Skin, Hip
(4)
Artery, pulmonary
(3)
Breast organoid
(3)
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Aorta, abdominal
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Ascites fluid
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dbGap Data Available:
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(3107)
Extended Clinical Data Available:
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(11469)
Age at Sampling (Years):
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35-44
(3386)
55-64
(3273)
25-34
(2682)
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(2452)
15-24
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5-14
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0-4
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75-89
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100+
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