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Search Results for -
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO
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DEFICIENCY OF CITRULLINE PHOSPHORYLASE
DEFICIENCY OF ORNITHINE CARBAMOYLTRANSFERASE
DEFICIENCY OF ORNITHINE TRANSCARBAMYLASE
OCT - ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY
OCT DEFICIENCY
OCTD
ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY
ORNITHINE TRANSCARBAMOYLASE DEFICIENCY
ORNITHINE TRANSCARBAMYLASE DEFICIENCY
OTC
OTC - ORNITHINE TRANSCARBAMYLASE DEFICIENCY
OTC DEFICIENCY
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Repository:
NIGMS Human Genetic Cell Repository
(7770)
NINDS Repository
(6308)
NIA Aging Cell Culture Repository
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HD Community Biorepository
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Heritable Diseases
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Human Variation
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CMD Specific
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CEPH
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Retinitis Pigmentosa Foundation Collection
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Repository Linkage Families
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FOXG1
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Old Order Amish Major Affective Disorder
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Apparently healthy iPSCs
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NHGRI Sample Repository for Human Genetic Research
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Affected:
At Risk
(6120)
Yes
(5022)
No
(1286)
Unknown
(75)
Mutation Data Available:
N
(10548)
Y
(4224)
Source:
B-Lymphocyte
(4542)
Whole Blood
(3958)
LCL
(2681)
Fibroblast
(957)
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(298)
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Other
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dbGap Data Available:
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(1081)
Extended Clinical Data Available:
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(8038)
Yes
(6734)
Age at Sampling (Years):
35-44
(2514)
45-54
(2053)
0-4
(1775)
25-34
(1762)
5-14
(1395)
55-64
(1318)
15-24
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