Family NIGMS00043 Members
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Records Return:
(5)
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Catalog ID | Description | Sex | Age | Race | Affected | Family Member | Relationship to Proband | Cell Type | Family |
GM28877 | ALACRIMA, ACHALASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; AAMR | Female | 15 MO | More than one race | Yes | 1 | proband | Fibroblast | NIGMS00043 |
GM28879 | ALACRIMA, ACHALASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; AAMR | Female | 38 YR | Asian | No | 2 | mother | Fibroblast | NIGMS00043 |
GM28880 | ALACRIMA, ACHALASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; AAMR | Female | 38 YR | Asian | No | 2 | mother | B-Lymphocyte | NIGMS00043 |
GM28881 | ALACRIMA, ACHALASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; AAMR | Male | 41 YR | White | No | 3 | father | Fibroblast | NIGMS00043 |
GM28882 | ALACRIMA, ACHALASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; AAMR | Male | 41 YR | White | No | 3 | father | B-Lymphocyte | NIGMS00043 |
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