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Search Results for -
3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY
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Also searched for:
3-METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY
3-METHYLCROTONYLGLYCINURIA I
BETA-METHYLCROTONYLGLYCINURIA TYPES I OR II - 210200 OR 210210
BETA-METHYLCROTONYLGLYCINURIA, TYPE 1
BMCC DEFICIENCY
DEFICIENCY OF METHYLCROTONOYL-COA CARBOXYLASE
DEFICIENCY OF METHYLCROTONOYL-COENZYME A CARBOXYLASE
MCC DEFICIENCY
MCC1 DEFICIENCY
MCCD TYPE 1
METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY
METHYLCROTONYL-COENZYME A CARBOXYLASE DEFICIENCY
METHYLCROTONYLGLYCINURIA TYPE I
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NHGRI Sample Repository for Human Genetic Research
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NHGRI Sample Repository for Human Genetic Research
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The 90+ Study
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CMD Specific
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Dystonia
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"Intra-abdominal fat and risk of disease in children and adolescents" study
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Alzheimer's Disease
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Venezuelan Huntington Disease
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Canadian Alzheimer Disease
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Disorders of the Urea Cycle
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Maturity-Onset Diabetes of the Young
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Retinitis Pigmentosa Foundation Collection
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human variation panel
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hybrid regional mapping panel
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Affected:
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No
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Mutation Data Available:
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Y
(6014)
No
(5)
Source:
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LCL
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Skin, Arm
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Whole embryo, Embryo
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Breast organoid
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Chest
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Endothelial
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Ewing sarcoma
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Fetal, Arm
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Heart, Unspecified
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Hydatidiform mole
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dbGap Data Available:
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(8310)
Extended Clinical Data Available:
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Yes
(25747)
Age at Sampling (Years):
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(7041)
45-54
(6379)
65-74
(6121)
35-44
(5243)
5-14
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25-34
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75-89
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